Canonical Allele Identifier: CA403987614

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464726T>A (hg19) ; chr19:g.10354050T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354050T>A , CM000681.2:g.10354050T>A	GRCh38
NC_000019.9:g.10464726T>A , CM000681.1:g.10464726T>A	GRCh37
NC_000019.8:g.10325726T>A	NCBI36
NG_007872.1:g.31523A>T , LRG_121:g.31523A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1249A>T	ENSP00000514307.1:n.*1249A>T
ENST00000525976.6:c.2900A>T	ENSP00000434831.2:p.Glu967Val
ENST00000527481.3:c.2900A>T	ENSP00000466340.2:p.Glu967Val
ENST00000529370.6:n.4276A>T
ENST00000529739.2:n.3314A>T
ENST00000530829.2:c.*2451A>T	ENSP00000436826.2:n.*2451A>T
ENST00000531836.6:c.2900A>T	ENSP00000436175.2:p.Glu967Val
ENST00000533334.2:c.*942A>T	ENSP00000432320.2:n.*942A>T
ENST00000534228.2:n.4359A>T
ENST00000699354.1:n.1002A>T
ENST00000699355.1:c.*2005A>T	ENSP00000514328.1:n.*2005A>T
ENST00000699356.1:n.3314A>T
ENST00000699357.1:n.4359A>T
ENST00000699358.1:c.2900A>T	ENSP00000514329.1:p.Glu967Val
ENST00000699359.1:c.106A>T
ENST00000699360.1:c.2900A>T	ENSP00000514331.1:p.Glu967Val
ENST00000699368.1:c.104A>T	ENSP00000514335.1:p.Glu35Val
ENST00000525621.6:c.2900A>T MANE Select	ENSP00000431885.1:p.Glu967Val
ENST00000264818.10:c.2900A>T	ENSP00000264818.6:p.Glu967Val
ENST00000524462.5:c.2345A>T	ENSP00000433203.1:p.Glu782Val
ENST00000525621.5:c.2900A>T	ENSP00000431885.1:p.Glu967Val
ENST00000527481.2:c.196A>T
ENST00000529412.1:n.572A>T
ENST00000529739.1:c.-427A>T	ENSP00000436155.1:n.-427A>T
ENST00000530560.5:c.329A>T	ENSP00000465291.1:p.Glu110Val
ENST00000592137.1:n.54A>T
NM_003331.4:c.2900A>T , LRG_121t1:c.2900A>T	NP_003322.3:p.Glu967Val
XM_011528245.1:c.2900A>T	XP_011526547.1:p.Glu967Val
XM_011528246.1:c.2603A>T	XP_011526548.1:p.Glu868Val
XM_011528247.1:c.2603A>T	XP_011526549.1:p.Glu868Val
XM_011528248.1:c.2900A>T	XP_011526550.1:p.Glu967Val
XM_011528249.1:c.1574A>T	XP_011526551.1:p.Glu525Val
XM_011528251.1:c.1157A>T	XP_011526553.1:p.Glu386Val
XM_011528246.3:c.2603A>T	XP_011526548.1:p.Glu868Val
XM_011528249.2:c.1574A>T	XP_011526551.1:p.Glu525Val
XR_001753750.1:n.3057A>T
XR_001753751.1:n.3057A>T
XR_002958353.1:n.3983A>T
NM_003331.5:c.2900A>T MANE Select	NP_003322.3:p.Glu967Val
NM_001385197.1:c.2900A>T	NP_001372126.1:p.Glu967Val
NM_001385198.1:c.2900A>T	NP_001372127.1:p.Glu967Val
NM_001385199.1:c.2714A>T	NP_001372128.1:p.Glu905Val
NM_001385200.1:c.2897A>T	NP_001372129.1:p.Glu966Val
NM_001385201.1:c.2702A>T	NP_001372130.1:p.Glu901Val
NM_001385202.1:c.2816A>T	NP_001372131.1:p.Glu939Val
NM_001385203.1:c.2981A>T	NP_001372132.1:p.Glu994Val
NM_001385204.1:c.3110A>T	NP_001372133.1:p.Glu1037Val
NM_001385205.1:c.2810A>T	NP_001372134.1:p.Glu937Val
NM_001385206.1:c.2774A>T	NP_001372135.1:p.Glu925Val
NM_001385207.1:c.2882A>T	NP_001372136.1:p.Glu961Val