Canonical Allele Identifier: CA2322389917

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10358111C= , CM000681.2:g.10358111C=	GRCh38
NC_000019.9:g.10468787C= , CM000681.1:g.10468787C=	GRCh37
NC_000019.8:g.10329787C=	NCBI36
NG_007872.1:g.27462G= , LRG_121:g.27462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*552G=	ENSP00000514307.1:n.*552G=
ENST00000525976.6:c.2203G=	ENSP00000434831.2:p.Val735=
ENST00000527481.3:c.2203G=	ENSP00000466340.2:p.Val735=
ENST00000529370.6:n.2534G=
ENST00000529739.2:n.2617G=
ENST00000530829.2:c.*1754G=	ENSP00000436826.2:n.*1754G=
ENST00000531836.6:c.2203G=	ENSP00000436175.2:p.Val735=
ENST00000533334.2:c.*245G=	ENSP00000432320.2:n.*245G=
ENST00000534228.2:n.2617G=
ENST00000699354.1:n.305G=
ENST00000699355.1:c.*263G=	ENSP00000514328.1:n.*263G=
ENST00000699356.1:n.2617G=
ENST00000699357.1:n.2617G=
ENST00000699358.1:c.2203G=	ENSP00000514329.1:p.Val735=
ENST00000699360.1:c.2203G=	ENSP00000514331.1:p.Val735=
ENST00000525621.6:c.2203G= MANE Select	ENSP00000431885.1:p.Val735=
ENST00000264818.10:c.2203G=	ENSP00000264818.6:p.Val735=
ENST00000524462.5:c.1648G=	ENSP00000433203.1:p.Val550=
ENST00000525621.5:c.2203G=	ENSP00000431885.1:p.Val735=
ENST00000529370.5:c.2203G=	ENSP00000432728.1:p.Val735=
ENST00000533334.1:c.492G=
NM_003331.4:c.2203G= , LRG_121t1:c.2203G=	NP_003322.3:p.Val735=
XM_011528245.1:c.2203G=	XP_011526547.1:p.Val735=
XM_011528246.1:c.1906G=	XP_011526548.1:p.Val636=
XM_011528247.1:c.1906G=	XP_011526549.1:p.Val636=
XM_011528248.1:c.2203G=	XP_011526550.1:p.Val735=
XM_011528249.1:c.877G=	XP_011526551.1:p.Val293=
XM_011528251.1:c.460G=	XP_011526553.1:p.Val154=
XM_011528246.3:c.1906G=	XP_011526548.1:p.Val636=
XM_011528249.2:c.877G=	XP_011526551.1:p.Val293=
XR_001753750.1:n.2360G=
XR_001753751.1:n.2360G=
XR_001753752.1:n.2472G=
XR_002958353.1:n.2241G=
NM_003331.5:c.2203G= MANE Select	NP_003322.3:p.Val735=
NM_001385197.1:c.2203G=	NP_001372126.1:p.Val735=
NM_001385198.1:c.2203G=	NP_001372127.1:p.Val735=
NM_001385199.1:c.2017G=	NP_001372128.1:p.Val673=
NM_001385200.1:c.2203G=	NP_001372129.1:p.Val735=
NM_001385201.1:c.2005G=	NP_001372130.1:p.Val669=
NM_001385202.1:c.2119G=	NP_001372131.1:p.Val707=
NM_001385203.1:c.2203G=	NP_001372132.1:p.Val735=
NM_001385204.1:c.2203G=	NP_001372133.1:p.Val735=
NM_001385205.1:c.2113G=	NP_001372134.1:p.Val705=
NM_001385206.1:c.2077G=	NP_001372135.1:p.Val693=
NM_001385207.1:c.2185G=	NP_001372136.1:p.Val729=