Canonical Allele Identifier: CA403988646

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464844C>T (hg19) ; chr19:g.10354168C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354168C>T , CM000681.2:g.10354168C>T	GRCh38
NC_000019.9:g.10464844C>T , CM000681.1:g.10464844C>T	GRCh37
NC_000019.8:g.10325844C>T	NCBI36
NG_007872.1:g.31405G>A , LRG_121:g.31405G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1131G>A	ENSP00000514307.1:n.*1131G>A
ENST00000525976.6:c.2782G>A	ENSP00000434831.2:p.Ala928Thr
ENST00000527481.3:c.2782G>A	ENSP00000466340.2:p.Ala928Thr
ENST00000529370.6:n.4158G>A
ENST00000529739.2:n.3196G>A
ENST00000530829.2:c.*2333G>A	ENSP00000436826.2:n.*2333G>A
ENST00000531836.6:c.2782G>A	ENSP00000436175.2:p.Ala928Thr
ENST00000533334.2:c.*824G>A	ENSP00000432320.2:n.*824G>A
ENST00000534228.2:n.4241G>A
ENST00000699354.1:n.884G>A
ENST00000699355.1:c.*1887G>A	ENSP00000514328.1:n.*1887G>A
ENST00000699356.1:n.3196G>A
ENST00000699357.1:n.4241G>A
ENST00000699358.1:c.2782G>A	ENSP00000514329.1:p.Ala928Thr
ENST00000699360.1:c.2782G>A	ENSP00000514331.1:p.Ala928Thr
ENST00000525621.6:c.2782G>A MANE Select	ENSP00000431885.1:p.Ala928Thr
ENST00000264818.10:c.2782G>A	ENSP00000264818.6:p.Ala928Thr
ENST00000524462.5:c.2227G>A	ENSP00000433203.1:p.Ala743Thr
ENST00000525621.5:c.2782G>A	ENSP00000431885.1:p.Ala928Thr
ENST00000527481.2:c.78G>A
ENST00000529412.1:n.454G>A
ENST00000530560.5:c.211G>A	ENSP00000465291.1:p.Ala71Thr
NM_003331.4:c.2782G>A , LRG_121t1:c.2782G>A	NP_003322.3:p.Ala928Thr
XM_011528245.1:c.2782G>A	XP_011526547.1:p.Ala928Thr
XM_011528246.1:c.2485G>A	XP_011526548.1:p.Ala829Thr
XM_011528247.1:c.2485G>A	XP_011526549.1:p.Ala829Thr
XM_011528248.1:c.2782G>A	XP_011526550.1:p.Ala928Thr
XM_011528249.1:c.1456G>A	XP_011526551.1:p.Ala486Thr
XM_011528251.1:c.1039G>A	XP_011526553.1:p.Ala347Thr
XM_011528246.3:c.2485G>A	XP_011526548.1:p.Ala829Thr
XM_011528249.2:c.1456G>A	XP_011526551.1:p.Ala486Thr
XR_001753750.1:n.2939G>A
XR_001753751.1:n.2939G>A
XR_002958353.1:n.3865G>A
NM_003331.5:c.2782G>A MANE Select	NP_003322.3:p.Ala928Thr
NM_001385197.1:c.2782G>A	NP_001372126.1:p.Ala928Thr
NM_001385198.1:c.2782G>A	NP_001372127.1:p.Ala928Thr
NM_001385199.1:c.2596G>A	NP_001372128.1:p.Ala866Thr
NM_001385200.1:c.2779G>A	NP_001372129.1:p.Ala927Thr
NM_001385201.1:c.2584G>A	NP_001372130.1:p.Ala862Thr
NM_001385202.1:c.2698G>A	NP_001372131.1:p.Ala900Thr
NM_001385203.1:c.2863G>A	NP_001372132.1:p.Ala955Thr
NM_001385204.1:c.2992G>A	NP_001372133.1:p.Ala998Thr
NM_001385205.1:c.2692G>A	NP_001372134.1:p.Ala898Thr
NM_001385206.1:c.2656G>A	NP_001372135.1:p.Ala886Thr
NM_001385207.1:c.2764G>A	NP_001372136.1:p.Ala922Thr