Canonical Allele Identifier: CA403987587

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464723T>A (hg19) ; chr19:g.10354047T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354047T>A , CM000681.2:g.10354047T>A	GRCh38
NC_000019.9:g.10464723T>A , CM000681.1:g.10464723T>A	GRCh37
NC_000019.8:g.10325723T>A	NCBI36
NG_007872.1:g.31526A>T , LRG_121:g.31526A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1252A>T	ENSP00000514307.1:n.*1252A>T
ENST00000525976.6:c.2903A>T	ENSP00000434831.2:p.Asp968Val
ENST00000527481.3:c.2903A>T	ENSP00000466340.2:p.Asp968Val
ENST00000529370.6:n.4279A>T
ENST00000529739.2:n.3317A>T
ENST00000530829.2:c.*2454A>T	ENSP00000436826.2:n.*2454A>T
ENST00000531836.6:c.2903A>T	ENSP00000436175.2:p.Asp968Val
ENST00000533334.2:c.*945A>T	ENSP00000432320.2:n.*945A>T
ENST00000534228.2:n.4362A>T
ENST00000699354.1:n.1005A>T
ENST00000699355.1:c.*2008A>T	ENSP00000514328.1:n.*2008A>T
ENST00000699356.1:n.3317A>T
ENST00000699357.1:n.4362A>T
ENST00000699358.1:c.2903A>T	ENSP00000514329.1:p.Asp968Val
ENST00000699359.1:c.109A>T
ENST00000699360.1:c.2903A>T	ENSP00000514331.1:p.Asp968Val
ENST00000699368.1:c.107A>T	ENSP00000514335.1:p.Asp36Val
ENST00000525621.6:c.2903A>T MANE Select	ENSP00000431885.1:p.Asp968Val
ENST00000264818.10:c.2903A>T	ENSP00000264818.6:p.Asp968Val
ENST00000524462.5:c.2348A>T	ENSP00000433203.1:p.Asp783Val
ENST00000525621.5:c.2903A>T	ENSP00000431885.1:p.Asp968Val
ENST00000527481.2:c.199A>T
ENST00000529412.1:n.575A>T
ENST00000529739.1:c.-424A>T	ENSP00000436155.1:n.-424A>T
ENST00000530560.5:c.332A>T	ENSP00000465291.1:p.Asp111Val
ENST00000592137.1:n.57A>T
NM_003331.4:c.2903A>T , LRG_121t1:c.2903A>T	NP_003322.3:p.Asp968Val
XM_011528245.1:c.2903A>T	XP_011526547.1:p.Asp968Val
XM_011528246.1:c.2606A>T	XP_011526548.1:p.Asp869Val
XM_011528247.1:c.2606A>T	XP_011526549.1:p.Asp869Val
XM_011528248.1:c.2903A>T	XP_011526550.1:p.Asp968Val
XM_011528249.1:c.1577A>T	XP_011526551.1:p.Asp526Val
XM_011528251.1:c.1160A>T	XP_011526553.1:p.Asp387Val
XM_011528246.3:c.2606A>T	XP_011526548.1:p.Asp869Val
XM_011528249.2:c.1577A>T	XP_011526551.1:p.Asp526Val
XR_001753750.1:n.3060A>T
XR_001753751.1:n.3060A>T
XR_002958353.1:n.3986A>T
NM_003331.5:c.2903A>T MANE Select	NP_003322.3:p.Asp968Val
NM_001385197.1:c.2903A>T	NP_001372126.1:p.Asp968Val
NM_001385198.1:c.2903A>T	NP_001372127.1:p.Asp968Val
NM_001385199.1:c.2717A>T	NP_001372128.1:p.Asp906Val
NM_001385200.1:c.2900A>T	NP_001372129.1:p.Asp967Val
NM_001385201.1:c.2705A>T	NP_001372130.1:p.Asp902Val
NM_001385202.1:c.2819A>T	NP_001372131.1:p.Asp940Val
NM_001385203.1:c.2984A>T	NP_001372132.1:p.Asp995Val
NM_001385204.1:c.3113A>T	NP_001372133.1:p.Asp1038Val
NM_001385205.1:c.2813A>T	NP_001372134.1:p.Asp938Val
NM_001385206.1:c.2777A>T	NP_001372135.1:p.Asp926Val
NM_001385207.1:c.2885A>T	NP_001372136.1:p.Asp962Val