Canonical Allele Identifier: CA403988478

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464821G>T (hg19) ; chr19:g.10354145G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354145G>T , CM000681.2:g.10354145G>T	GRCh38
NC_000019.9:g.10464821G>T , CM000681.1:g.10464821G>T	GRCh37
NC_000019.8:g.10325821G>T	NCBI36
NG_007872.1:g.31428C>A , LRG_121:g.31428C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1154C>A	ENSP00000514307.1:n.*1154C>A
ENST00000525976.6:c.2805C>A	ENSP00000434831.2:p.Asp935Glu
ENST00000527481.3:c.2805C>A	ENSP00000466340.2:p.Asp935Glu
ENST00000529370.6:n.4181C>A
ENST00000529739.2:n.3219C>A
ENST00000530829.2:c.*2356C>A	ENSP00000436826.2:n.*2356C>A
ENST00000531836.6:c.2805C>A	ENSP00000436175.2:p.Asp935Glu
ENST00000533334.2:c.*847C>A	ENSP00000432320.2:n.*847C>A
ENST00000534228.2:n.4264C>A
ENST00000699354.1:n.907C>A
ENST00000699355.1:c.*1910C>A	ENSP00000514328.1:n.*1910C>A
ENST00000699356.1:n.3219C>A
ENST00000699357.1:n.4264C>A
ENST00000699358.1:c.2805C>A	ENSP00000514329.1:p.Asp935Glu
ENST00000699359.1:c.11C>A
ENST00000699360.1:c.2805C>A	ENSP00000514331.1:p.Asp935Glu
ENST00000699368.1:c.9C>A	ENSP00000514335.1:p.Asp3Glu
ENST00000525621.6:c.2805C>A MANE Select	ENSP00000431885.1:p.Asp935Glu
ENST00000264818.10:c.2805C>A	ENSP00000264818.6:p.Asp935Glu
ENST00000524462.5:c.2250C>A	ENSP00000433203.1:p.Asp750Glu
ENST00000525621.5:c.2805C>A	ENSP00000431885.1:p.Asp935Glu
ENST00000527481.2:c.101C>A
ENST00000529412.1:n.477C>A
ENST00000530560.5:c.234C>A	ENSP00000465291.1:p.Asp78Glu
NM_003331.4:c.2805C>A , LRG_121t1:c.2805C>A	NP_003322.3:p.Asp935Glu
XM_011528245.1:c.2805C>A	XP_011526547.1:p.Asp935Glu
XM_011528246.1:c.2508C>A	XP_011526548.1:p.Asp836Glu
XM_011528247.1:c.2508C>A	XP_011526549.1:p.Asp836Glu
XM_011528248.1:c.2805C>A	XP_011526550.1:p.Asp935Glu
XM_011528249.1:c.1479C>A	XP_011526551.1:p.Asp493Glu
XM_011528251.1:c.1062C>A	XP_011526553.1:p.Asp354Glu
XM_011528246.3:c.2508C>A	XP_011526548.1:p.Asp836Glu
XM_011528249.2:c.1479C>A	XP_011526551.1:p.Asp493Glu
XR_001753750.1:n.2962C>A
XR_001753751.1:n.2962C>A
XR_002958353.1:n.3888C>A
NM_003331.5:c.2805C>A MANE Select	NP_003322.3:p.Asp935Glu
NM_001385197.1:c.2805C>A	NP_001372126.1:p.Asp935Glu
NM_001385198.1:c.2805C>A	NP_001372127.1:p.Asp935Glu
NM_001385199.1:c.2619C>A	NP_001372128.1:p.Asp873Glu
NM_001385200.1:c.2802C>A	NP_001372129.1:p.Asp934Glu
NM_001385201.1:c.2607C>A	NP_001372130.1:p.Asp869Glu
NM_001385202.1:c.2721C>A	NP_001372131.1:p.Asp907Glu
NM_001385203.1:c.2886C>A	NP_001372132.1:p.Asp962Glu
NM_001385204.1:c.3015C>A	NP_001372133.1:p.Asp1005Glu
NM_001385205.1:c.2715C>A	NP_001372134.1:p.Asp905Glu
NM_001385206.1:c.2679C>A	NP_001372135.1:p.Asp893Glu
NM_001385207.1:c.2787C>A	NP_001372136.1:p.Asp929Glu