Canonical Allele Identifier: CA505373691

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464797G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354121G>T , CM000681.2:g.10354121G>T	GRCh38
NC_000019.9:g.10464797G>T , CM000681.1:g.10464797G>T	GRCh37
NC_000019.8:g.10325797G>T	NCBI36
NG_007872.1:g.31452C>A , LRG_121:g.31452C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1178C>A	ENSP00000514307.1:n.*1178C>A
ENST00000525976.6:c.2829C>A	ENSP00000434831.2:p.Gly943=
ENST00000527481.3:c.2829C>A	ENSP00000466340.2:p.Gly943=
ENST00000529370.6:n.4205C>A
ENST00000529739.2:n.3243C>A
ENST00000530829.2:c.*2380C>A	ENSP00000436826.2:n.*2380C>A
ENST00000531836.6:c.2829C>A	ENSP00000436175.2:p.Gly943=
ENST00000533334.2:c.*871C>A	ENSP00000432320.2:n.*871C>A
ENST00000534228.2:n.4288C>A
ENST00000699354.1:n.931C>A
ENST00000699355.1:c.*1934C>A	ENSP00000514328.1:n.*1934C>A
ENST00000699356.1:n.3243C>A
ENST00000699357.1:n.4288C>A
ENST00000699358.1:c.2829C>A	ENSP00000514329.1:p.Gly943=
ENST00000699359.1:c.35C>A
ENST00000699360.1:c.2829C>A	ENSP00000514331.1:p.Gly943=
ENST00000699368.1:c.33C>A	ENSP00000514335.1:p.Gly11=
ENST00000525621.6:c.2829C>A MANE Select	ENSP00000431885.1:p.Gly943=
ENST00000264818.10:c.2829C>A	ENSP00000264818.6:p.Gly943=
ENST00000524462.5:c.2274C>A	ENSP00000433203.1:p.Gly758=
ENST00000525621.5:c.2829C>A	ENSP00000431885.1:p.Gly943=
ENST00000527481.2:c.125C>A
ENST00000529412.1:n.501C>A
ENST00000530560.5:c.258C>A	ENSP00000465291.1:p.Gly86=
NM_003331.4:c.2829C>A , LRG_121t1:c.2829C>A	NP_003322.3:p.Gly943=
XM_011528245.1:c.2829C>A	XP_011526547.1:p.Gly943=
XM_011528246.1:c.2532C>A	XP_011526548.1:p.Gly844=
XM_011528247.1:c.2532C>A	XP_011526549.1:p.Gly844=
XM_011528248.1:c.2829C>A	XP_011526550.1:p.Gly943=
XM_011528249.1:c.1503C>A	XP_011526551.1:p.Gly501=
XM_011528251.1:c.1086C>A	XP_011526553.1:p.Gly362=
XM_011528246.3:c.2532C>A	XP_011526548.1:p.Gly844=
XM_011528249.2:c.1503C>A	XP_011526551.1:p.Gly501=
XR_001753750.1:n.2986C>A
XR_001753751.1:n.2986C>A
XR_002958353.1:n.3912C>A
NM_003331.5:c.2829C>A MANE Select	NP_003322.3:p.Gly943=
NM_001385197.1:c.2829C>A	NP_001372126.1:p.Gly943=
NM_001385198.1:c.2829C>A	NP_001372127.1:p.Gly943=
NM_001385199.1:c.2643C>A	NP_001372128.1:p.Gly881=
NM_001385200.1:c.2826C>A	NP_001372129.1:p.Gly942=
NM_001385201.1:c.2631C>A	NP_001372130.1:p.Gly877=
NM_001385202.1:c.2745C>A	NP_001372131.1:p.Gly915=
NM_001385203.1:c.2910C>A	NP_001372132.1:p.Gly970=
NM_001385204.1:c.3039C>A	NP_001372133.1:p.Gly1013=
NM_001385205.1:c.2739C>A	NP_001372134.1:p.Gly913=
NM_001385206.1:c.2703C>A	NP_001372135.1:p.Gly901=
NM_001385207.1:c.2811C>A	NP_001372136.1:p.Gly937=