Canonical Allele Identifier: CA505373402

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464734G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354058G>A , CM000681.2:g.10354058G>A	GRCh38
NC_000019.9:g.10464734G>A , CM000681.1:g.10464734G>A	GRCh37
NC_000019.8:g.10325734G>A	NCBI36
NG_007872.1:g.31515C>T , LRG_121:g.31515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1241C>T	ENSP00000514307.1:n.*1241C>T
ENST00000525976.6:c.2892C>T	ENSP00000434831.2:p.Gly964=
ENST00000527481.3:c.2892C>T	ENSP00000466340.2:p.Gly964=
ENST00000529370.6:n.4268C>T
ENST00000529739.2:n.3306C>T
ENST00000530829.2:c.*2443C>T	ENSP00000436826.2:n.*2443C>T
ENST00000531836.6:c.2892C>T	ENSP00000436175.2:p.Gly964=
ENST00000533334.2:c.*934C>T	ENSP00000432320.2:n.*934C>T
ENST00000534228.2:n.4351C>T
ENST00000699354.1:n.994C>T
ENST00000699355.1:c.*1997C>T	ENSP00000514328.1:n.*1997C>T
ENST00000699356.1:n.3306C>T
ENST00000699357.1:n.4351C>T
ENST00000699358.1:c.2892C>T	ENSP00000514329.1:p.Gly964=
ENST00000699359.1:c.98C>T
ENST00000699360.1:c.2892C>T	ENSP00000514331.1:p.Gly964=
ENST00000699368.1:c.96C>T	ENSP00000514335.1:p.Gly32=
ENST00000525621.6:c.2892C>T MANE Select	ENSP00000431885.1:p.Gly964=
ENST00000264818.10:c.2892C>T	ENSP00000264818.6:p.Gly964=
ENST00000524462.5:c.2337C>T	ENSP00000433203.1:p.Gly779=
ENST00000525621.5:c.2892C>T	ENSP00000431885.1:p.Gly964=
ENST00000527481.2:c.188C>T
ENST00000529412.1:n.564C>T
ENST00000529739.1:c.-435C>T	ENSP00000436155.1:n.-435C>T
ENST00000530560.5:c.321C>T	ENSP00000465291.1:p.Gly107=
ENST00000592137.1:n.46C>T
NM_003331.4:c.2892C>T , LRG_121t1:c.2892C>T	NP_003322.3:p.Gly964=
XM_011528245.1:c.2892C>T	XP_011526547.1:p.Gly964=
XM_011528246.1:c.2595C>T	XP_011526548.1:p.Gly865=
XM_011528247.1:c.2595C>T	XP_011526549.1:p.Gly865=
XM_011528248.1:c.2892C>T	XP_011526550.1:p.Gly964=
XM_011528249.1:c.1566C>T	XP_011526551.1:p.Gly522=
XM_011528251.1:c.1149C>T	XP_011526553.1:p.Gly383=
XM_011528246.3:c.2595C>T	XP_011526548.1:p.Gly865=
XM_011528249.2:c.1566C>T	XP_011526551.1:p.Gly522=
XR_001753750.1:n.3049C>T
XR_001753751.1:n.3049C>T
XR_002958353.1:n.3975C>T
NM_003331.5:c.2892C>T MANE Select	NP_003322.3:p.Gly964=
NM_001385197.1:c.2892C>T	NP_001372126.1:p.Gly964=
NM_001385198.1:c.2892C>T	NP_001372127.1:p.Gly964=
NM_001385199.1:c.2706C>T	NP_001372128.1:p.Gly902=
NM_001385200.1:c.2889C>T	NP_001372129.1:p.Gly963=
NM_001385201.1:c.2694C>T	NP_001372130.1:p.Gly898=
NM_001385202.1:c.2808C>T	NP_001372131.1:p.Gly936=
NM_001385203.1:c.2973C>T	NP_001372132.1:p.Gly991=
NM_001385204.1:c.3102C>T	NP_001372133.1:p.Gly1034=
NM_001385205.1:c.2802C>T	NP_001372134.1:p.Gly934=
NM_001385206.1:c.2766C>T	NP_001372135.1:p.Gly922=
NM_001385207.1:c.2874C>T	NP_001372136.1:p.Gly958=