Canonical Allele Identifier: CA403998518

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468784A>C (hg19) ; chr19:g.10358108A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10358108A>C , CM000681.2:g.10358108A>C	GRCh38
NC_000019.9:g.10468784A>C , CM000681.1:g.10468784A>C	GRCh37
NC_000019.8:g.10329784A>C	NCBI36
NG_007872.1:g.27465T>G , LRG_121:g.27465T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*555T>G	ENSP00000514307.1:n.*555T>G
ENST00000525976.6:c.2206T>G	ENSP00000434831.2:p.Cys736Gly
ENST00000527481.3:c.2206T>G	ENSP00000466340.2:p.Cys736Gly
ENST00000529370.6:n.2537T>G
ENST00000529739.2:n.2620T>G
ENST00000530829.2:c.*1757T>G	ENSP00000436826.2:n.*1757T>G
ENST00000531836.6:c.2206T>G	ENSP00000436175.2:p.Cys736Gly
ENST00000533334.2:c.*248T>G	ENSP00000432320.2:n.*248T>G
ENST00000534228.2:n.2620T>G
ENST00000699354.1:n.308T>G
ENST00000699355.1:c.*266T>G	ENSP00000514328.1:n.*266T>G
ENST00000699356.1:n.2620T>G
ENST00000699357.1:n.2620T>G
ENST00000699358.1:c.2206T>G	ENSP00000514329.1:p.Cys736Gly
ENST00000699360.1:c.2206T>G	ENSP00000514331.1:p.Cys736Gly
ENST00000525621.6:c.2206T>G MANE Select	ENSP00000431885.1:p.Cys736Gly
ENST00000264818.10:c.2206T>G	ENSP00000264818.6:p.Cys736Gly
ENST00000524462.5:c.1651T>G	ENSP00000433203.1:p.Cys551Gly
ENST00000525621.5:c.2206T>G	ENSP00000431885.1:p.Cys736Gly
ENST00000529370.5:c.2206T>G	ENSP00000432728.1:p.Cys736Gly
ENST00000533334.1:c.495T>G
NM_003331.4:c.2206T>G , LRG_121t1:c.2206T>G	NP_003322.3:p.Cys736Gly
XM_011528245.1:c.2206T>G	XP_011526547.1:p.Cys736Gly
XM_011528246.1:c.1909T>G	XP_011526548.1:p.Cys637Gly
XM_011528247.1:c.1909T>G	XP_011526549.1:p.Cys637Gly
XM_011528248.1:c.2206T>G	XP_011526550.1:p.Cys736Gly
XM_011528249.1:c.880T>G	XP_011526551.1:p.Cys294Gly
XM_011528251.1:c.463T>G	XP_011526553.1:p.Cys155Gly
XM_011528246.3:c.1909T>G	XP_011526548.1:p.Cys637Gly
XM_011528249.2:c.880T>G	XP_011526551.1:p.Cys294Gly
XR_001753750.1:n.2363T>G
XR_001753751.1:n.2363T>G
XR_001753752.1:n.2475T>G
XR_002958353.1:n.2244T>G
NM_003331.5:c.2206T>G MANE Select	NP_003322.3:p.Cys736Gly
NM_001385197.1:c.2206T>G	NP_001372126.1:p.Cys736Gly
NM_001385198.1:c.2206T>G	NP_001372127.1:p.Cys736Gly
NM_001385199.1:c.2020T>G	NP_001372128.1:p.Cys674Gly
NM_001385200.1:c.2206T>G	NP_001372129.1:p.Cys736Gly
NM_001385201.1:c.2008T>G	NP_001372130.1:p.Cys670Gly
NM_001385202.1:c.2122T>G	NP_001372131.1:p.Cys708Gly
NM_001385203.1:c.2206T>G	NP_001372132.1:p.Cys736Gly
NM_001385204.1:c.2206T>G	NP_001372133.1:p.Cys736Gly
NM_001385205.1:c.2116T>G	NP_001372134.1:p.Cys706Gly
NM_001385206.1:c.2080T>G	NP_001372135.1:p.Cys694Gly
NM_001385207.1:c.2188T>G	NP_001372136.1:p.Cys730Gly