Canonical Allele Identifier: CA403987823

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464754G>A (hg19) ; chr19:g.10354078G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354078G>A , CM000681.2:g.10354078G>A	GRCh38
NC_000019.9:g.10464754G>A , CM000681.1:g.10464754G>A	GRCh37
NC_000019.8:g.10325754G>A	NCBI36
NG_007872.1:g.31495C>T , LRG_121:g.31495C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1221C>T	ENSP00000514307.1:n.*1221C>T
ENST00000525976.6:c.2872C>T	ENSP00000434831.2:p.His958Tyr
ENST00000527481.3:c.2872C>T	ENSP00000466340.2:p.His958Tyr
ENST00000529370.6:n.4248C>T
ENST00000529739.2:n.3286C>T
ENST00000530829.2:c.*2423C>T	ENSP00000436826.2:n.*2423C>T
ENST00000531836.6:c.2872C>T	ENSP00000436175.2:p.His958Tyr
ENST00000533334.2:c.*914C>T	ENSP00000432320.2:n.*914C>T
ENST00000534228.2:n.4331C>T
ENST00000699354.1:n.974C>T
ENST00000699355.1:c.*1977C>T	ENSP00000514328.1:n.*1977C>T
ENST00000699356.1:n.3286C>T
ENST00000699357.1:n.4331C>T
ENST00000699358.1:c.2872C>T	ENSP00000514329.1:p.His958Tyr
ENST00000699359.1:c.78C>T
ENST00000699360.1:c.2872C>T	ENSP00000514331.1:p.His958Tyr
ENST00000699368.1:c.76C>T	ENSP00000514335.1:p.His26Tyr
ENST00000525621.6:c.2872C>T MANE Select	ENSP00000431885.1:p.His958Tyr
ENST00000264818.10:c.2872C>T	ENSP00000264818.6:p.His958Tyr
ENST00000524462.5:c.2317C>T	ENSP00000433203.1:p.His773Tyr
ENST00000525621.5:c.2872C>T	ENSP00000431885.1:p.His958Tyr
ENST00000527481.2:c.168C>T
ENST00000529412.1:n.544C>T
ENST00000529739.1:c.-455C>T	ENSP00000436155.1:n.-455C>T
ENST00000530560.5:c.301C>T	ENSP00000465291.1:p.His101Tyr
ENST00000592137.1:n.26C>T
NM_003331.4:c.2872C>T , LRG_121t1:c.2872C>T	NP_003322.3:p.His958Tyr
XM_011528245.1:c.2872C>T	XP_011526547.1:p.His958Tyr
XM_011528246.1:c.2575C>T	XP_011526548.1:p.His859Tyr
XM_011528247.1:c.2575C>T	XP_011526549.1:p.His859Tyr
XM_011528248.1:c.2872C>T	XP_011526550.1:p.His958Tyr
XM_011528249.1:c.1546C>T	XP_011526551.1:p.His516Tyr
XM_011528251.1:c.1129C>T	XP_011526553.1:p.His377Tyr
XM_011528246.3:c.2575C>T	XP_011526548.1:p.His859Tyr
XM_011528249.2:c.1546C>T	XP_011526551.1:p.His516Tyr
XR_001753750.1:n.3029C>T
XR_001753751.1:n.3029C>T
XR_002958353.1:n.3955C>T
NM_003331.5:c.2872C>T MANE Select	NP_003322.3:p.His958Tyr
NM_001385197.1:c.2872C>T	NP_001372126.1:p.His958Tyr
NM_001385198.1:c.2872C>T	NP_001372127.1:p.His958Tyr
NM_001385199.1:c.2686C>T	NP_001372128.1:p.His896Tyr
NM_001385200.1:c.2869C>T	NP_001372129.1:p.His957Tyr
NM_001385201.1:c.2674C>T	NP_001372130.1:p.His892Tyr
NM_001385202.1:c.2788C>T	NP_001372131.1:p.His930Tyr
NM_001385203.1:c.2953C>T	NP_001372132.1:p.His985Tyr
NM_001385204.1:c.3082C>T	NP_001372133.1:p.His1028Tyr
NM_001385205.1:c.2782C>T	NP_001372134.1:p.His928Tyr
NM_001385206.1:c.2746C>T	NP_001372135.1:p.His916Tyr
NM_001385207.1:c.2854C>T	NP_001372136.1:p.His952Tyr