Canonical Allele Identifier: CA403987641

Gene: TYK2

Linked Data

• dbSNP Id: rs763754692
• MyVariant Identifiers: chr19:g.10464730A>T (hg19) ; chr19:g.10354054A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354054A>T , CM000681.2:g.10354054A>T	GRCh38
NC_000019.9:g.10464730A>T , CM000681.1:g.10464730A>T	GRCh37
NC_000019.8:g.10325730A>T	NCBI36
NG_007872.1:g.31519T>A , LRG_121:g.31519T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1245T>A	ENSP00000514307.1:n.*1245T>A
ENST00000525976.6:c.2896T>A	ENSP00000434831.2:p.Cys966Ser
ENST00000527481.3:c.2896T>A	ENSP00000466340.2:p.Cys966Ser
ENST00000529370.6:n.4272T>A
ENST00000529739.2:n.3310T>A
ENST00000530829.2:c.*2447T>A	ENSP00000436826.2:n.*2447T>A
ENST00000531836.6:c.2896T>A	ENSP00000436175.2:p.Cys966Ser
ENST00000533334.2:c.*938T>A	ENSP00000432320.2:n.*938T>A
ENST00000534228.2:n.4355T>A
ENST00000699354.1:n.998T>A
ENST00000699355.1:c.*2001T>A	ENSP00000514328.1:n.*2001T>A
ENST00000699356.1:n.3310T>A
ENST00000699357.1:n.4355T>A
ENST00000699358.1:c.2896T>A	ENSP00000514329.1:p.Cys966Ser
ENST00000699359.1:c.102T>A
ENST00000699360.1:c.2896T>A	ENSP00000514331.1:p.Cys966Ser
ENST00000699368.1:c.100T>A	ENSP00000514335.1:p.Cys34Ser
ENST00000525621.6:c.2896T>A MANE Select	ENSP00000431885.1:p.Cys966Ser
ENST00000264818.10:c.2896T>A	ENSP00000264818.6:p.Cys966Ser
ENST00000524462.5:c.2341T>A	ENSP00000433203.1:p.Cys781Ser
ENST00000525621.5:c.2896T>A	ENSP00000431885.1:p.Cys966Ser
ENST00000527481.2:c.192T>A
ENST00000529412.1:n.568T>A
ENST00000529739.1:c.-431T>A	ENSP00000436155.1:n.-431T>A
ENST00000530560.5:c.325T>A	ENSP00000465291.1:p.Cys109Ser
ENST00000592137.1:n.50T>A
NM_003331.4:c.2896T>A , LRG_121t1:c.2896T>A	NP_003322.3:p.Cys966Ser
XM_011528245.1:c.2896T>A	XP_011526547.1:p.Cys966Ser
XM_011528246.1:c.2599T>A	XP_011526548.1:p.Cys867Ser
XM_011528247.1:c.2599T>A	XP_011526549.1:p.Cys867Ser
XM_011528248.1:c.2896T>A	XP_011526550.1:p.Cys966Ser
XM_011528249.1:c.1570T>A	XP_011526551.1:p.Cys524Ser
XM_011528251.1:c.1153T>A	XP_011526553.1:p.Cys385Ser
XM_011528246.3:c.2599T>A	XP_011526548.1:p.Cys867Ser
XM_011528249.2:c.1570T>A	XP_011526551.1:p.Cys524Ser
XR_001753750.1:n.3053T>A
XR_001753751.1:n.3053T>A
XR_002958353.1:n.3979T>A
NM_003331.5:c.2896T>A MANE Select	NP_003322.3:p.Cys966Ser
NM_001385197.1:c.2896T>A	NP_001372126.1:p.Cys966Ser
NM_001385198.1:c.2896T>A	NP_001372127.1:p.Cys966Ser
NM_001385199.1:c.2710T>A	NP_001372128.1:p.Cys904Ser
NM_001385200.1:c.2893T>A	NP_001372129.1:p.Cys965Ser
NM_001385201.1:c.2698T>A	NP_001372130.1:p.Cys900Ser
NM_001385202.1:c.2812T>A	NP_001372131.1:p.Cys938Ser
NM_001385203.1:c.2977T>A	NP_001372132.1:p.Cys993Ser
NM_001385204.1:c.3106T>A	NP_001372133.1:p.Cys1036Ser
NM_001385205.1:c.2806T>A	NP_001372134.1:p.Cys936Ser
NM_001385206.1:c.2770T>A	NP_001372135.1:p.Cys924Ser
NM_001385207.1:c.2878T>A	NP_001372136.1:p.Cys960Ser