Canonical Allele Identifier: CA403988636

Gene: TYK2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1131G>T	ENSP00000514307.1:n.*1131G>T
ENST00000525976.6:c.2782G>T	ENSP00000434831.2:p.Ala928Ser
ENST00000527481.3:c.2782G>T	ENSP00000466340.2:p.Ala928Ser
ENST00000529370.6:n.4158G>T
ENST00000529739.2:n.3196G>T
ENST00000530829.2:c.*2333G>T	ENSP00000436826.2:n.*2333G>T
ENST00000531836.6:c.2782G>T	ENSP00000436175.2:p.Ala928Ser
ENST00000533334.2:c.*824G>T	ENSP00000432320.2:n.*824G>T
ENST00000534228.2:n.4241G>T
ENST00000699354.1:n.884G>T
ENST00000699355.1:c.*1887G>T	ENSP00000514328.1:n.*1887G>T
ENST00000699356.1:n.3196G>T
ENST00000699357.1:n.4241G>T
ENST00000699358.1:c.2782G>T	ENSP00000514329.1:p.Ala928Ser
ENST00000699360.1:c.2782G>T	ENSP00000514331.1:p.Ala928Ser
ENST00000525621.6:c.2782G>T MANE Select	ENSP00000431885.1:p.Ala928Ser
ENST00000264818.10:c.2782G>T	ENSP00000264818.6:p.Ala928Ser
ENST00000524462.5:c.2227G>T	ENSP00000433203.1:p.Ala743Ser
ENST00000525621.5:c.2782G>T	ENSP00000431885.1:p.Ala928Ser
ENST00000527481.2:c.78G>T
ENST00000529412.1:n.454G>T
ENST00000530560.5:c.211G>T	ENSP00000465291.1:p.Ala71Ser
NM_003331.4:c.2782G>T , LRG_121t1:c.2782G>T	NP_003322.3:p.Ala928Ser
XM_011528245.1:c.2782G>T	XP_011526547.1:p.Ala928Ser
XM_011528246.1:c.2485G>T	XP_011526548.1:p.Ala829Ser
XM_011528247.1:c.2485G>T	XP_011526549.1:p.Ala829Ser
XM_011528248.1:c.2782G>T	XP_011526550.1:p.Ala928Ser
XM_011528249.1:c.1456G>T	XP_011526551.1:p.Ala486Ser
XM_011528251.1:c.1039G>T	XP_011526553.1:p.Ala347Ser
XM_011528246.3:c.2485G>T	XP_011526548.1:p.Ala829Ser
XM_011528249.2:c.1456G>T	XP_011526551.1:p.Ala486Ser
XR_001753750.1:n.2939G>T
XR_001753751.1:n.2939G>T
XR_002958353.1:n.3865G>T
NM_003331.5:c.2782G>T MANE Select	NP_003322.3:p.Ala928Ser
NM_001385197.1:c.2782G>T	NP_001372126.1:p.Ala928Ser
NM_001385198.1:c.2782G>T	NP_001372127.1:p.Ala928Ser
NM_001385199.1:c.2596G>T	NP_001372128.1:p.Ala866Ser
NM_001385200.1:c.2779G>T	NP_001372129.1:p.Ala927Ser
NM_001385201.1:c.2584G>T	NP_001372130.1:p.Ala862Ser
NM_001385202.1:c.2698G>T	NP_001372131.1:p.Ala900Ser
NM_001385203.1:c.2863G>T	NP_001372132.1:p.Ala955Ser
NM_001385204.1:c.2992G>T	NP_001372133.1:p.Ala998Ser
NM_001385205.1:c.2692G>T	NP_001372134.1:p.Ala898Ser
NM_001385206.1:c.2656G>T	NP_001372135.1:p.Ala886Ser
NM_001385207.1:c.2764G>T	NP_001372136.1:p.Ala922Ser