Canonical Allele Identifier: CA2582370259

Gene: TYK2

Linked Data

• gnomAD v4: 19-10352804-C-CTAGGCCCCACCCCCGCACG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352804_10352805insTAGGCCCCACCCCCGCACG , CM000681.2:g.10352804_10352805insTAGGCCCCACCCCCGCACG	GRCh38
NC_000019.9:g.10463480_10463481insTAGGCCCCACCCCCGCACG , CM000681.1:g.10463480_10463481insTAGGCCCCACCCCCGCACG	GRCh37
NC_000019.8:g.10324480_10324481insTAGGCCCCACCCCCGCACG	NCBI36
NG_007872.1:g.32768_32769insCGTGCGGGGGTGGGGCCTA , LRG_121:g.32768_32769insCGTGCGGGGGTGGGGCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1549+121_*1549+122insCGTGCGGGGGTGGGGCCTA	ENSP00000514307.1:n.*1549+121_*1549+122insCGTGCGGGGGTGGGGCCTA...
ENST00000525976.6:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	ENSP00000434831.2:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
ENST00000527481.3:c.3081+121_3081+122insCGTGCGGGGGTGGGGCCTA	ENSP00000466340.2:n.3081+121_3081+122insCGTGCGGGGGTGGGGCCTA
ENST00000529370.6:n.4576+121_4576+122insCGTGCGGGGGTGGGGCCTA
ENST00000529739.2:n.4009+121_4009+122insCGTGCGGGGGTGGGGCCTA
ENST00000530829.2:c.*2751+121_*2751+122insCGTGCGGGGGTGGGGCCTA	ENSP00000436826.2:n.*2751+121_*2751+122insCGTGCGGGGGTGGGGCCTA...
ENST00000531836.6:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	ENSP00000436175.2:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
ENST00000533334.2:c.*1242+121_*1242+122insCGTGCGGGGGTGGGGCCTA	ENSP00000432320.2:n.*1242+121_*1242+122insCGTGCGGGGGTGGGGCCTA...
ENST00000534228.2:n.5054+121_5054+122insCGTGCGGGGGTGGGGCCTA
ENST00000699354.1:n.1302+121_1302+122insCGTGCGGGGGTGGGGCCTA
ENST00000699355.1:c.*2700+121_*2700+122insCGTGCGGGGGTGGGGCCTA	ENSP00000514328.1:n.*2700+121_*2700+122insCGTGCGGGGGTGGGGCCTA...
ENST00000699356.1:n.4009+121_4009+122insCGTGCGGGGGTGGGGCCTA
ENST00000699357.1:n.5054+121_5054+122insCGTGCGGGGGTGGGGCCTA
ENST00000699358.1:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	ENSP00000514329.1:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
ENST00000699359.1:c.374+153_374+154insCGTGCGGGGGTGGGGCCTA
ENST00000699360.1:c.3158+163_3158+164insCGTGCGGGGGTGGGGCCTA	ENSP00000514331.1:n.3158+163_3158+164insCGTGCGGGGGTGGGGCCTA
ENST00000699362.1:c.97-254_97-253insCGTGCGGGGGTGGGGCCTA	ENSP00000514332.1:n.97-254_97-253insCGTGCGGGGGTGGGGCCTA
ENST00000699363.1:c.97-254_97-253insCGTGCGGGGGTGGGGCCTA	ENSP00000514333.1:n.97-254_97-253insCGTGCGGGGGTGGGGCCTA
ENST00000699364.1:n.200+121_200+122insCGTGCGGGGGTGGGGCCTA
ENST00000699365.1:c.269+121_269+122insCGTGCGGGGGTGGGGCCTA	ENSP00000514334.1:n.269+121_269+122insCGTGCGGGGGTGGGGCCTA
ENST00000699366.1:n.111+1009_111+1010insCGTGCGGGGGTGGGGCCTA
ENST00000699367.1:n.111+1009_111+1010insCGTGCGGGGGTGGGGCCTA
ENST00000699368.1:c.687+121_687+122insCGTGCGGGGGTGGGGCCTA	ENSP00000514335.1:n.687+121_687+122insCGTGCGGGGGTGGGGCCTA
ENST00000525621.6:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA MANE Select	ENSP00000431885.1:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
ENST00000264818.10:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	ENSP00000264818.6:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
ENST00000524462.5:c.2645+121_2645+122insCGTGCGGGGGTGGGGCCTA	ENSP00000433203.1:n.2645+121_2645+122insCGTGCGGGGGTGGGGCCTA
ENST00000525621.5:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	ENSP00000431885.1:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
ENST00000527481.2:c.377+121_377+122insCGTGCGGGGGTGGGGCCTA
ENST00000529422.1:n.116+217_116+218insCGTGCGGGGGTGGGGCCTA
ENST00000529739.1:c.269+121_269+122insCGTGCGGGGGTGGGGCCTA	ENSP00000436155.1:n.269+121_269+122insCGTGCGGGGGTGGGGCCTA
ENST00000530220.1:n.331+121_331+122insCGTGCGGGGGTGGGGCCTA
ENST00000530560.5:c.337+1237_337+1238insCGTGCGGGGGTGGGGCCTA	ENSP00000465291.1:n.337+1237_337+1238insCGTGCGGGGGTGGGGCCTA
ENST00000592137.1:n.354+121_354+122insCGTGCGGGGGTGGGGCCTA
NM_003331.4:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA , LRG_121t1:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	NP_003322.3:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
XM_011528245.1:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	XP_011526547.1:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
XM_011528246.1:c.2903+121_2903+122insCGTGCGGGGGTGGGGCCTA	XP_011526548.1:n.2903+121_2903+122insCGTGCGGGGGTGGGGCCTA
XM_011528247.1:c.2903+121_2903+122insCGTGCGGGGGTGGGGCCTA	XP_011526549.1:n.2903+121_2903+122insCGTGCGGGGGTGGGGCCTA
XM_011528248.1:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	XP_011526550.1:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
XM_011528249.1:c.1874+121_1874+122insCGTGCGGGGGTGGGGCCTA	XP_011526551.1:n.1874+121_1874+122insCGTGCGGGGGTGGGGCCTA
XM_011528251.1:c.1457+121_1457+122insCGTGCGGGGGTGGGGCCTA	XP_011526553.1:n.1457+121_1457+122insCGTGCGGGGGTGGGGCCTA
XM_011528246.3:c.2903+121_2903+122insCGTGCGGGGGTGGGGCCTA	XP_011526548.1:n.2903+121_2903+122insCGTGCGGGGGTGGGGCCTA
XM_011528249.2:c.1874+121_1874+122insCGTGCGGGGGTGGGGCCTA	XP_011526551.1:n.1874+121_1874+122insCGTGCGGGGGTGGGGCCTA
XR_001753750.1:n.3357+121_3357+122insCGTGCGGGGGTGGGGCCTA
XR_001753751.1:n.3752+121_3752+122insCGTGCGGGGGTGGGGCCTA
XR_002958353.1:n.4678+121_4678+122insCGTGCGGGGGTGGGGCCTA
NM_003331.5:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA MANE Select	NP_003322.3:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
NM_001385197.1:c.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA	NP_001372126.1:n.3200+121_3200+122insCGTGCGGGGGTGGGGCCTA
NM_001385198.1:c.3168+153_3168+154insCGTGCGGGGGTGGGGCCTA	NP_001372127.1:n.3168+153_3168+154insCGTGCGGGGGTGGGGCCTA
NM_001385199.1:c.3014+121_3014+122insCGTGCGGGGGTGGGGCCTA	NP_001372128.1:n.3014+121_3014+122insCGTGCGGGGGTGGGGCCTA
NM_001385200.1:c.3197+121_3197+122insCGTGCGGGGGTGGGGCCTA	NP_001372129.1:n.3197+121_3197+122insCGTGCGGGGGTGGGGCCTA
NM_001385201.1:c.3002+121_3002+122insCGTGCGGGGGTGGGGCCTA	NP_001372130.1:n.3002+121_3002+122insCGTGCGGGGGTGGGGCCTA
NM_001385202.1:c.3116+121_3116+122insCGTGCGGGGGTGGGGCCTA	NP_001372131.1:n.3116+121_3116+122insCGTGCGGGGGTGGGGCCTA
NM_001385203.1:c.3281+121_3281+122insCGTGCGGGGGTGGGGCCTA	NP_001372132.1:n.3281+121_3281+122insCGTGCGGGGGTGGGGCCTA
NM_001385204.1:c.3410+121_3410+122insCGTGCGGGGGTGGGGCCTA	NP_001372133.1:n.3410+121_3410+122insCGTGCGGGGGTGGGGCCTA
NM_001385205.1:c.3110+121_3110+122insCGTGCGGGGGTGGGGCCTA	NP_001372134.1:n.3110+121_3110+122insCGTGCGGGGGTGGGGCCTA
NM_001385206.1:c.3074+121_3074+122insCGTGCGGGGGTGGGGCCTA	NP_001372135.1:n.3074+121_3074+122insCGTGCGGGGGTGGGGCCTA
NM_001385207.1:c.3182+121_3182+122insCGTGCGGGGGTGGGGCCTA	NP_001372136.1:n.3182+121_3182+122insCGTGCGGGGGTGGGGCCTA