Canonical Allele Identifier: CA403996076

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468588A>C (hg19) ; chr19:g.10357912A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357912A>C , CM000681.2:g.10357912A>C	GRCh38
NC_000019.9:g.10468588A>C , CM000681.1:g.10468588A>C	GRCh37
NC_000019.8:g.10329588A>C	NCBI36
NG_007872.1:g.27661T>G , LRG_121:g.27661T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*667T>G	ENSP00000514307.1:n.*667T>G
ENST00000525976.6:c.2318T>G	ENSP00000434831.2:p.Val773Gly
ENST00000527481.3:c.2318T>G	ENSP00000466340.2:p.Val773Gly
ENST00000529370.6:n.2649T>G
ENST00000529739.2:n.2732T>G
ENST00000530829.2:c.*1869T>G	ENSP00000436826.2:n.*1869T>G
ENST00000531836.6:c.2318T>G	ENSP00000436175.2:p.Val773Gly
ENST00000533334.2:c.*360T>G	ENSP00000432320.2:n.*360T>G
ENST00000534228.2:n.2732T>G
ENST00000699354.1:n.420T>G
ENST00000699355.1:c.*378T>G	ENSP00000514328.1:n.*378T>G
ENST00000699356.1:n.2732T>G
ENST00000699357.1:n.2732T>G
ENST00000699358.1:c.2318T>G	ENSP00000514329.1:p.Val773Gly
ENST00000699360.1:c.2318T>G	ENSP00000514331.1:p.Val773Gly
ENST00000525621.6:c.2318T>G MANE Select	ENSP00000431885.1:p.Val773Gly
ENST00000264818.10:c.2318T>G	ENSP00000264818.6:p.Val773Gly
ENST00000524462.5:c.1763T>G	ENSP00000433203.1:p.Val588Gly
ENST00000525621.5:c.2318T>G	ENSP00000431885.1:p.Val773Gly
ENST00000529370.5:c.2318T>G	ENSP00000432728.1:p.Val773Gly
ENST00000533334.1:c.607T>G
NM_003331.4:c.2318T>G , LRG_121t1:c.2318T>G	NP_003322.3:p.Val773Gly
XM_011528245.1:c.2318T>G	XP_011526547.1:p.Val773Gly
XM_011528246.1:c.2021T>G	XP_011526548.1:p.Val674Gly
XM_011528247.1:c.2021T>G	XP_011526549.1:p.Val674Gly
XM_011528248.1:c.2318T>G	XP_011526550.1:p.Val773Gly
XM_011528249.1:c.992T>G	XP_011526551.1:p.Val331Gly
XM_011528251.1:c.575T>G	XP_011526553.1:p.Val192Gly
XM_011528246.3:c.2021T>G	XP_011526548.1:p.Val674Gly
XM_011528249.2:c.992T>G	XP_011526551.1:p.Val331Gly
XR_001753750.1:n.2475T>G
XR_001753751.1:n.2475T>G
XR_001753752.1:n.2587T>G
XR_002958353.1:n.2356T>G
NM_003331.5:c.2318T>G MANE Select	NP_003322.3:p.Val773Gly
NM_001385197.1:c.2318T>G	NP_001372126.1:p.Val773Gly
NM_001385198.1:c.2318T>G	NP_001372127.1:p.Val773Gly
NM_001385199.1:c.2132T>G	NP_001372128.1:p.Val711Gly
NM_001385200.1:c.2318T>G	NP_001372129.1:p.Val773Gly
NM_001385201.1:c.2120T>G	NP_001372130.1:p.Val707Gly
NM_001385202.1:c.2234T>G	NP_001372131.1:p.Val745Gly
NM_001385203.1:c.2318T>G	NP_001372132.1:p.Val773Gly
NM_001385204.1:c.2318T>G	NP_001372133.1:p.Val773Gly
NM_001385205.1:c.2228T>G	NP_001372134.1:p.Val743Gly
NM_001385206.1:c.2192T>G	NP_001372135.1:p.Val731Gly
NM_001385207.1:c.2300T>G	NP_001372136.1:p.Val767Gly