Canonical Allele Identifier: CA403987660

Gene: TYK2

Linked Data

• gnomAD v4: 19-10354059-C-T
• MyVariant Identifiers: chr19:g.10464735C>T (hg19) ; chr19:g.10354059C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354059C>T , CM000681.2:g.10354059C>T	GRCh38
NC_000019.9:g.10464735C>T , CM000681.1:g.10464735C>T	GRCh37
NC_000019.8:g.10325735C>T	NCBI36
NG_007872.1:g.31514G>A , LRG_121:g.31514G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1240G>A	ENSP00000514307.1:n.*1240G>A
ENST00000525976.6:c.2891G>A	ENSP00000434831.2:p.Gly964Asp
ENST00000527481.3:c.2891G>A	ENSP00000466340.2:p.Gly964Asp
ENST00000529370.6:n.4267G>A
ENST00000529739.2:n.3305G>A
ENST00000530829.2:c.*2442G>A	ENSP00000436826.2:n.*2442G>A
ENST00000531836.6:c.2891G>A	ENSP00000436175.2:p.Gly964Asp
ENST00000533334.2:c.*933G>A	ENSP00000432320.2:n.*933G>A
ENST00000534228.2:n.4350G>A
ENST00000699354.1:n.993G>A
ENST00000699355.1:c.*1996G>A	ENSP00000514328.1:n.*1996G>A
ENST00000699356.1:n.3305G>A
ENST00000699357.1:n.4350G>A
ENST00000699358.1:c.2891G>A	ENSP00000514329.1:p.Gly964Asp
ENST00000699359.1:c.97G>A
ENST00000699360.1:c.2891G>A	ENSP00000514331.1:p.Gly964Asp
ENST00000699368.1:c.95G>A	ENSP00000514335.1:p.Gly32Asp
ENST00000525621.6:c.2891G>A MANE Select	ENSP00000431885.1:p.Gly964Asp
ENST00000264818.10:c.2891G>A	ENSP00000264818.6:p.Gly964Asp
ENST00000524462.5:c.2336G>A	ENSP00000433203.1:p.Gly779Asp
ENST00000525621.5:c.2891G>A	ENSP00000431885.1:p.Gly964Asp
ENST00000527481.2:c.187G>A
ENST00000529412.1:n.563G>A
ENST00000529739.1:c.-436G>A	ENSP00000436155.1:n.-436G>A
ENST00000530560.5:c.320G>A	ENSP00000465291.1:p.Gly107Asp
ENST00000592137.1:n.45G>A
NM_003331.4:c.2891G>A , LRG_121t1:c.2891G>A	NP_003322.3:p.Gly964Asp
XM_011528245.1:c.2891G>A	XP_011526547.1:p.Gly964Asp
XM_011528246.1:c.2594G>A	XP_011526548.1:p.Gly865Asp
XM_011528247.1:c.2594G>A	XP_011526549.1:p.Gly865Asp
XM_011528248.1:c.2891G>A	XP_011526550.1:p.Gly964Asp
XM_011528249.1:c.1565G>A	XP_011526551.1:p.Gly522Asp
XM_011528251.1:c.1148G>A	XP_011526553.1:p.Gly383Asp
XM_011528246.3:c.2594G>A	XP_011526548.1:p.Gly865Asp
XM_011528249.2:c.1565G>A	XP_011526551.1:p.Gly522Asp
XR_001753750.1:n.3048G>A
XR_001753751.1:n.3048G>A
XR_002958353.1:n.3974G>A
NM_003331.5:c.2891G>A MANE Select	NP_003322.3:p.Gly964Asp
NM_001385197.1:c.2891G>A	NP_001372126.1:p.Gly964Asp
NM_001385198.1:c.2891G>A	NP_001372127.1:p.Gly964Asp
NM_001385199.1:c.2705G>A	NP_001372128.1:p.Gly902Asp
NM_001385200.1:c.2888G>A	NP_001372129.1:p.Gly963Asp
NM_001385201.1:c.2693G>A	NP_001372130.1:p.Gly898Asp
NM_001385202.1:c.2807G>A	NP_001372131.1:p.Gly936Asp
NM_001385203.1:c.2972G>A	NP_001372132.1:p.Gly991Asp
NM_001385204.1:c.3101G>A	NP_001372133.1:p.Gly1034Asp
NM_001385205.1:c.2801G>A	NP_001372134.1:p.Gly934Asp
NM_001385206.1:c.2765G>A	NP_001372135.1:p.Gly922Asp
NM_001385207.1:c.2873G>A	NP_001372136.1:p.Gly958Asp