Canonical Allele Identifier: CA403987667

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464736C>G (hg19) ; chr19:g.10354060C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354060C>G , CM000681.2:g.10354060C>G	GRCh38
NC_000019.9:g.10464736C>G , CM000681.1:g.10464736C>G	GRCh37
NC_000019.8:g.10325736C>G	NCBI36
NG_007872.1:g.31513G>C , LRG_121:g.31513G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1239G>C	ENSP00000514307.1:n.*1239G>C
ENST00000525976.6:c.2890G>C	ENSP00000434831.2:p.Gly964Arg
ENST00000527481.3:c.2890G>C	ENSP00000466340.2:p.Gly964Arg
ENST00000529370.6:n.4266G>C
ENST00000529739.2:n.3304G>C
ENST00000530829.2:c.*2441G>C	ENSP00000436826.2:n.*2441G>C
ENST00000531836.6:c.2890G>C	ENSP00000436175.2:p.Gly964Arg
ENST00000533334.2:c.*932G>C	ENSP00000432320.2:n.*932G>C
ENST00000534228.2:n.4349G>C
ENST00000699354.1:n.992G>C
ENST00000699355.1:c.*1995G>C	ENSP00000514328.1:n.*1995G>C
ENST00000699356.1:n.3304G>C
ENST00000699357.1:n.4349G>C
ENST00000699358.1:c.2890G>C	ENSP00000514329.1:p.Gly964Arg
ENST00000699359.1:c.96G>C
ENST00000699360.1:c.2890G>C	ENSP00000514331.1:p.Gly964Arg
ENST00000699368.1:c.94G>C	ENSP00000514335.1:p.Gly32Arg
ENST00000525621.6:c.2890G>C MANE Select	ENSP00000431885.1:p.Gly964Arg
ENST00000264818.10:c.2890G>C	ENSP00000264818.6:p.Gly964Arg
ENST00000524462.5:c.2335G>C	ENSP00000433203.1:p.Gly779Arg
ENST00000525621.5:c.2890G>C	ENSP00000431885.1:p.Gly964Arg
ENST00000527481.2:c.186G>C
ENST00000529412.1:n.562G>C
ENST00000529739.1:c.-437G>C	ENSP00000436155.1:n.-437G>C
ENST00000530560.5:c.319G>C	ENSP00000465291.1:p.Gly107Arg
ENST00000592137.1:n.44G>C
NM_003331.4:c.2890G>C , LRG_121t1:c.2890G>C	NP_003322.3:p.Gly964Arg
XM_011528245.1:c.2890G>C	XP_011526547.1:p.Gly964Arg
XM_011528246.1:c.2593G>C	XP_011526548.1:p.Gly865Arg
XM_011528247.1:c.2593G>C	XP_011526549.1:p.Gly865Arg
XM_011528248.1:c.2890G>C	XP_011526550.1:p.Gly964Arg
XM_011528249.1:c.1564G>C	XP_011526551.1:p.Gly522Arg
XM_011528251.1:c.1147G>C	XP_011526553.1:p.Gly383Arg
XM_011528246.3:c.2593G>C	XP_011526548.1:p.Gly865Arg
XM_011528249.2:c.1564G>C	XP_011526551.1:p.Gly522Arg
XR_001753750.1:n.3047G>C
XR_001753751.1:n.3047G>C
XR_002958353.1:n.3973G>C
NM_003331.5:c.2890G>C MANE Select	NP_003322.3:p.Gly964Arg
NM_001385197.1:c.2890G>C	NP_001372126.1:p.Gly964Arg
NM_001385198.1:c.2890G>C	NP_001372127.1:p.Gly964Arg
NM_001385199.1:c.2704G>C	NP_001372128.1:p.Gly902Arg
NM_001385200.1:c.2887G>C	NP_001372129.1:p.Gly963Arg
NM_001385201.1:c.2692G>C	NP_001372130.1:p.Gly898Arg
NM_001385202.1:c.2806G>C	NP_001372131.1:p.Gly936Arg
NM_001385203.1:c.2971G>C	NP_001372132.1:p.Gly991Arg
NM_001385204.1:c.3100G>C	NP_001372133.1:p.Gly1034Arg
NM_001385205.1:c.2800G>C	NP_001372134.1:p.Gly934Arg
NM_001385206.1:c.2764G>C	NP_001372135.1:p.Gly922Arg
NM_001385207.1:c.2872G>C	NP_001372136.1:p.Gly958Arg