Canonical Allele Identifier: CA2322387555

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352794_10352799delinsACCCCC , CM000681.2:g.10352794_10352799delinsACCCCC	GRCh38
NC_000019.9:g.10463470_10463475delinsACCCCC , CM000681.1:g.10463470_10463475delinsACCCCC	GRCh37
NC_000019.8:g.10324470_10324475delinsACCCCC	NCBI36
NG_007872.1:g.32774_32779delinsGGGGGT , LRG_121:g.32774_32779delinsGGGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1549+127_*1549+132delinsGGGGGT	ENSP00000514307.1:n.*1549+127_*1549+132delinsGGGGGT
ENST00000525976.6:c.3200+127_3200+132delinsGGGGGT	ENSP00000434831.2:n.3200+127_3200+132delinsGGGGGT
ENST00000527481.3:c.3081+127_3081+132delinsGGGGGT	ENSP00000466340.2:n.3081+127_3081+132delinsGGGGGT
ENST00000529370.6:n.4576+127_4576+132delinsGGGGGT
ENST00000529739.2:n.4009+127_4009+132delinsGGGGGT
ENST00000530829.2:c.*2751+127_*2751+132delinsGGGGGT	ENSP00000436826.2:n.*2751+127_*2751+132delinsGGGGGT
ENST00000531836.6:c.3200+127_3200+132delinsGGGGGT	ENSP00000436175.2:n.3200+127_3200+132delinsGGGGGT
ENST00000533334.2:c.*1242+127_*1242+132delinsGGGGGT	ENSP00000432320.2:n.*1242+127_*1242+132delinsGGGGGT
ENST00000534228.2:n.5054+127_5054+132delinsGGGGGT
ENST00000699354.1:n.1302+127_1302+132delinsGGGGGT
ENST00000699355.1:c.*2700+127_*2700+132delinsGGGGGT	ENSP00000514328.1:n.*2700+127_*2700+132delinsGGGGGT
ENST00000699356.1:n.4009+127_4009+132delinsGGGGGT
ENST00000699357.1:n.5054+127_5054+132delinsGGGGGT
ENST00000699358.1:c.3200+127_3200+132delinsGGGGGT	ENSP00000514329.1:n.3200+127_3200+132delinsGGGGGT
ENST00000699359.1:c.374+159_374+164delinsGGGGGT
ENST00000699360.1:c.3158+169_3158+174delinsGGGGGT	ENSP00000514331.1:n.3158+169_3158+174delinsGGGGGT
ENST00000699362.1:c.97-248_97-243delinsGGGGGT	ENSP00000514332.1:n.97-248_97-243delinsGGGGGT
ENST00000699363.1:c.97-248_97-243delinsGGGGGT	ENSP00000514333.1:n.97-248_97-243delinsGGGGGT
ENST00000699364.1:n.200+127_200+132delinsGGGGGT
ENST00000699365.1:c.269+127_269+132delinsGGGGGT	ENSP00000514334.1:n.269+127_269+132delinsGGGGGT
ENST00000699366.1:n.111+1015_111+1020delinsGGGGGT
ENST00000699367.1:n.111+1015_111+1020delinsGGGGGT
ENST00000699368.1:c.687+127_687+132delinsGGGGGT	ENSP00000514335.1:n.687+127_687+132delinsGGGGGT
ENST00000525621.6:c.3200+127_3200+132delinsGGGGGT MANE Select	ENSP00000431885.1:n.3200+127_3200+132delinsGGGGGT
ENST00000264818.10:c.3200+127_3200+132delinsGGGGGT	ENSP00000264818.6:n.3200+127_3200+132delinsGGGGGT
ENST00000524462.5:c.2645+127_2645+132delinsGGGGGT	ENSP00000433203.1:n.2645+127_2645+132delinsGGGGGT
ENST00000525621.5:c.3200+127_3200+132delinsGGGGGT	ENSP00000431885.1:n.3200+127_3200+132delinsGGGGGT
ENST00000527481.2:c.377+127_377+132delinsGGGGGT
ENST00000529422.1:n.116+223_116+228delinsGGGGGT
ENST00000529739.1:c.269+127_269+132delinsGGGGGT	ENSP00000436155.1:n.269+127_269+132delinsGGGGGT
ENST00000530220.1:n.331+127_331+132delinsGGGGGT
ENST00000530560.5:c.337+1243_337+1248delinsGGGGGT	ENSP00000465291.1:n.337+1243_337+1248delinsGGGGGT
ENST00000592137.1:n.354+127_354+132delinsGGGGGT
NM_003331.4:c.3200+127_3200+132delinsGGGGGT , LRG_121t1:c.3200+127_3200+132delinsGGGGGT	NP_003322.3:n.3200+127_3200+132delinsGGGGGT
XM_011528245.1:c.3200+127_3200+132delinsGGGGGT	XP_011526547.1:n.3200+127_3200+132delinsGGGGGT
XM_011528246.1:c.2903+127_2903+132delinsGGGGGT	XP_011526548.1:n.2903+127_2903+132delinsGGGGGT
XM_011528247.1:c.2903+127_2903+132delinsGGGGGT	XP_011526549.1:n.2903+127_2903+132delinsGGGGGT
XM_011528248.1:c.3200+127_3200+132delinsGGGGGT	XP_011526550.1:n.3200+127_3200+132delinsGGGGGT
XM_011528249.1:c.1874+127_1874+132delinsGGGGGT	XP_011526551.1:n.1874+127_1874+132delinsGGGGGT
XM_011528251.1:c.1457+127_1457+132delinsGGGGGT	XP_011526553.1:n.1457+127_1457+132delinsGGGGGT
XM_011528246.3:c.2903+127_2903+132delinsGGGGGT	XP_011526548.1:n.2903+127_2903+132delinsGGGGGT
XM_011528249.2:c.1874+127_1874+132delinsGGGGGT	XP_011526551.1:n.1874+127_1874+132delinsGGGGGT
XR_001753750.1:n.3357+127_3357+132delinsGGGGGT
XR_001753751.1:n.3752+127_3752+132delinsGGGGGT
XR_002958353.1:n.4678+127_4678+132delinsGGGGGT
NM_003331.5:c.3200+127_3200+132delinsGGGGGT MANE Select	NP_003322.3:n.3200+127_3200+132delinsGGGGGT
NM_001385197.1:c.3200+127_3200+132delinsGGGGGT	NP_001372126.1:n.3200+127_3200+132delinsGGGGGT
NM_001385198.1:c.3168+159_3168+164delinsGGGGGT	NP_001372127.1:n.3168+159_3168+164delinsGGGGGT
NM_001385199.1:c.3014+127_3014+132delinsGGGGGT	NP_001372128.1:n.3014+127_3014+132delinsGGGGGT
NM_001385200.1:c.3197+127_3197+132delinsGGGGGT	NP_001372129.1:n.3197+127_3197+132delinsGGGGGT
NM_001385201.1:c.3002+127_3002+132delinsGGGGGT	NP_001372130.1:n.3002+127_3002+132delinsGGGGGT
NM_001385202.1:c.3116+127_3116+132delinsGGGGGT	NP_001372131.1:n.3116+127_3116+132delinsGGGGGT
NM_001385203.1:c.3281+127_3281+132delinsGGGGGT	NP_001372132.1:n.3281+127_3281+132delinsGGGGGT
NM_001385204.1:c.3410+127_3410+132delinsGGGGGT	NP_001372133.1:n.3410+127_3410+132delinsGGGGGT
NM_001385205.1:c.3110+127_3110+132delinsGGGGGT	NP_001372134.1:n.3110+127_3110+132delinsGGGGGT
NM_001385206.1:c.3074+127_3074+132delinsGGGGGT	NP_001372135.1:n.3074+127_3074+132delinsGGGGGT
NM_001385207.1:c.3182+127_3182+132delinsGGGGGT	NP_001372136.1:n.3182+127_3182+132delinsGGGGGT