Canonical Allele Identifier: CA403987717

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464743C>A (hg19) ; chr19:g.10354067C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354067C>A , CM000681.2:g.10354067C>A	GRCh38
NC_000019.9:g.10464743C>A , CM000681.1:g.10464743C>A	GRCh37
NC_000019.8:g.10325743C>A	NCBI36
NG_007872.1:g.31506G>T , LRG_121:g.31506G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1232G>T	ENSP00000514307.1:n.*1232G>T
ENST00000525976.6:c.2883G>T	ENSP00000434831.2:p.Lys961Asn
ENST00000527481.3:c.2883G>T	ENSP00000466340.2:p.Lys961Asn
ENST00000529370.6:n.4259G>T
ENST00000529739.2:n.3297G>T
ENST00000530829.2:c.*2434G>T	ENSP00000436826.2:n.*2434G>T
ENST00000531836.6:c.2883G>T	ENSP00000436175.2:p.Lys961Asn
ENST00000533334.2:c.*925G>T	ENSP00000432320.2:n.*925G>T
ENST00000534228.2:n.4342G>T
ENST00000699354.1:n.985G>T
ENST00000699355.1:c.*1988G>T	ENSP00000514328.1:n.*1988G>T
ENST00000699356.1:n.3297G>T
ENST00000699357.1:n.4342G>T
ENST00000699358.1:c.2883G>T	ENSP00000514329.1:p.Lys961Asn
ENST00000699359.1:c.89G>T
ENST00000699360.1:c.2883G>T	ENSP00000514331.1:p.Lys961Asn
ENST00000699368.1:c.87G>T	ENSP00000514335.1:p.Lys29Asn
ENST00000525621.6:c.2883G>T MANE Select	ENSP00000431885.1:p.Lys961Asn
ENST00000264818.10:c.2883G>T	ENSP00000264818.6:p.Lys961Asn
ENST00000524462.5:c.2328G>T	ENSP00000433203.1:p.Lys776Asn
ENST00000525621.5:c.2883G>T	ENSP00000431885.1:p.Lys961Asn
ENST00000527481.2:c.179G>T
ENST00000529412.1:n.555G>T
ENST00000529739.1:c.-444G>T	ENSP00000436155.1:n.-444G>T
ENST00000530560.5:c.312G>T	ENSP00000465291.1:p.Lys104Asn
ENST00000592137.1:n.37G>T
NM_003331.4:c.2883G>T , LRG_121t1:c.2883G>T	NP_003322.3:p.Lys961Asn
XM_011528245.1:c.2883G>T	XP_011526547.1:p.Lys961Asn
XM_011528246.1:c.2586G>T	XP_011526548.1:p.Lys862Asn
XM_011528247.1:c.2586G>T	XP_011526549.1:p.Lys862Asn
XM_011528248.1:c.2883G>T	XP_011526550.1:p.Lys961Asn
XM_011528249.1:c.1557G>T	XP_011526551.1:p.Lys519Asn
XM_011528251.1:c.1140G>T	XP_011526553.1:p.Lys380Asn
XM_011528246.3:c.2586G>T	XP_011526548.1:p.Lys862Asn
XM_011528249.2:c.1557G>T	XP_011526551.1:p.Lys519Asn
XR_001753750.1:n.3040G>T
XR_001753751.1:n.3040G>T
XR_002958353.1:n.3966G>T
NM_003331.5:c.2883G>T MANE Select	NP_003322.3:p.Lys961Asn
NM_001385197.1:c.2883G>T	NP_001372126.1:p.Lys961Asn
NM_001385198.1:c.2883G>T	NP_001372127.1:p.Lys961Asn
NM_001385199.1:c.2697G>T	NP_001372128.1:p.Lys899Asn
NM_001385200.1:c.2880G>T	NP_001372129.1:p.Lys960Asn
NM_001385201.1:c.2685G>T	NP_001372130.1:p.Lys895Asn
NM_001385202.1:c.2799G>T	NP_001372131.1:p.Lys933Asn
NM_001385203.1:c.2964G>T	NP_001372132.1:p.Lys988Asn
NM_001385204.1:c.3093G>T	NP_001372133.1:p.Lys1031Asn
NM_001385205.1:c.2793G>T	NP_001372134.1:p.Lys931Asn
NM_001385206.1:c.2757G>T	NP_001372135.1:p.Lys919Asn
NM_001385207.1:c.2865G>T	NP_001372136.1:p.Lys955Asn