Canonical Allele Identifier: CA2322389751

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357749_10357751delinsGTC , CM000681.2:g.10357749_10357751delinsGTC	GRCh38
NC_000019.9:g.10468425_10468427delinsGTC , CM000681.1:g.10468425_10468427delinsGTC	GRCh37
NC_000019.8:g.10329425_10329427delinsGTC	NCBI36
NG_007872.1:g.27822_27824delinsGAC , LRG_121:g.27822_27824delinsGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*815+13_*815+15delinsGAC	ENSP00000514307.1:n.*815+13_*815+15delinsGAC
ENST00000525976.6:c.2466+13_2466+15delinsGAC	ENSP00000434831.2:n.2466+13_2466+15delinsGAC
ENST00000527481.3:c.2466+13_2466+15delinsGAC	ENSP00000466340.2:n.2466+13_2466+15delinsGAC
ENST00000529370.6:n.2810_2812delinsGAC
ENST00000529739.2:n.2880+13_2880+15delinsGAC
ENST00000530829.2:c.*2017+13_*2017+15delinsGAC	ENSP00000436826.2:n.*2017+13_*2017+15delinsGAC
ENST00000531836.6:c.2466+13_2466+15delinsGAC	ENSP00000436175.2:n.2466+13_2466+15delinsGAC
ENST00000533334.2:c.*508+13_*508+15delinsGAC	ENSP00000432320.2:n.*508+13_*508+15delinsGAC
ENST00000534228.2:n.2893_2895delinsGAC
ENST00000699354.1:n.568+13_568+15delinsGAC
ENST00000699355.1:c.*539_*541delinsGAC	ENSP00000514328.1:n.*539_*541delinsGAC
ENST00000699356.1:n.2880+13_2880+15delinsGAC
ENST00000699357.1:n.2893_2895delinsGAC
ENST00000699358.1:c.2466+13_2466+15delinsGAC	ENSP00000514329.1:n.2466+13_2466+15delinsGAC
ENST00000699360.1:c.2466+13_2466+15delinsGAC	ENSP00000514331.1:n.2466+13_2466+15delinsGAC
ENST00000525621.6:c.2466+13_2466+15delinsGAC MANE Select	ENSP00000431885.1:n.2466+13_2466+15delinsGAC
ENST00000264818.10:c.2466+13_2466+15delinsGAC	ENSP00000264818.6:n.2466+13_2466+15delinsGAC
ENST00000524462.5:c.1911+13_1911+15delinsGAC	ENSP00000433203.1:n.1911+13_1911+15delinsGAC
ENST00000525621.5:c.2466+13_2466+15delinsGAC	ENSP00000431885.1:n.2466+13_2466+15delinsGAC
ENST00000529370.5:c.2479_2481delinsGAC	ENSP00000432728.1:p.Asp827=
ENST00000529412.1:n.138+13_138+15delinsGAC
NM_003331.4:c.2466+13_2466+15delinsGAC , LRG_121t1:c.2466+13_2466+15delinsGAC	NP_003322.3:n.2466+13_2466+15delinsGAC
XM_011528245.1:c.2466+13_2466+15delinsGAC	XP_011526547.1:n.2466+13_2466+15delinsGAC
XM_011528246.1:c.2169+13_2169+15delinsGAC	XP_011526548.1:n.2169+13_2169+15delinsGAC
XM_011528247.1:c.2169+13_2169+15delinsGAC	XP_011526549.1:n.2169+13_2169+15delinsGAC
XM_011528248.1:c.2466+13_2466+15delinsGAC	XP_011526550.1:n.2466+13_2466+15delinsGAC
XM_011528249.1:c.1140+13_1140+15delinsGAC	XP_011526551.1:n.1140+13_1140+15delinsGAC
XM_011528251.1:c.723+13_723+15delinsGAC	XP_011526553.1:n.723+13_723+15delinsGAC
XM_011528246.3:c.2169+13_2169+15delinsGAC	XP_011526548.1:n.2169+13_2169+15delinsGAC
XM_011528249.2:c.1140+13_1140+15delinsGAC	XP_011526551.1:n.1140+13_1140+15delinsGAC
XR_001753750.1:n.2623+13_2623+15delinsGAC
XR_001753751.1:n.2623+13_2623+15delinsGAC
XR_002958353.1:n.2517_2519delinsGAC
NM_003331.5:c.2466+13_2466+15delinsGAC MANE Select	NP_003322.3:n.2466+13_2466+15delinsGAC
NM_001385197.1:c.2466+13_2466+15delinsGAC	NP_001372126.1:n.2466+13_2466+15delinsGAC
NM_001385198.1:c.2466+13_2466+15delinsGAC	NP_001372127.1:n.2466+13_2466+15delinsGAC
NM_001385199.1:c.2280+13_2280+15delinsGAC	NP_001372128.1:n.2280+13_2280+15delinsGAC
NM_001385200.1:c.2466+13_2466+15delinsGAC	NP_001372129.1:n.2466+13_2466+15delinsGAC
NM_001385201.1:c.2268+13_2268+15delinsGAC	NP_001372130.1:n.2268+13_2268+15delinsGAC
NM_001385202.1:c.2382+13_2382+15delinsGAC	NP_001372131.1:n.2382+13_2382+15delinsGAC
NM_001385203.1:c.2466+13_2466+15delinsGAC	NP_001372132.1:n.2466+13_2466+15delinsGAC
NM_001385204.1:c.2479_2481delinsGAC	NP_001372133.1:p.Asp827=
NM_001385205.1:c.2376+13_2376+15delinsGAC	NP_001372134.1:n.2376+13_2376+15delinsGAC
NM_001385206.1:c.2340+13_2340+15delinsGAC	NP_001372135.1:n.2340+13_2340+15delinsGAC
NM_001385207.1:c.2448+13_2448+15delinsGAC	NP_001372136.1:n.2448+13_2448+15delinsGAC