Canonical Allele Identifier: CA403996063

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10468585T>C (hg19) ; chr19:g.10357909T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10357909T>C , CM000681.2:g.10357909T>C	GRCh38
NC_000019.9:g.10468585T>C , CM000681.1:g.10468585T>C	GRCh37
NC_000019.8:g.10329585T>C	NCBI36
NG_007872.1:g.27664A>G , LRG_121:g.27664A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*670A>G	ENSP00000514307.1:n.*670A>G
ENST00000525976.6:c.2321A>G	ENSP00000434831.2:p.Glu774Gly
ENST00000527481.3:c.2321A>G	ENSP00000466340.2:p.Glu774Gly
ENST00000529370.6:n.2652A>G
ENST00000529739.2:n.2735A>G
ENST00000530829.2:c.*1872A>G	ENSP00000436826.2:n.*1872A>G
ENST00000531836.6:c.2321A>G	ENSP00000436175.2:p.Glu774Gly
ENST00000533334.2:c.*363A>G	ENSP00000432320.2:n.*363A>G
ENST00000534228.2:n.2735A>G
ENST00000699354.1:n.423A>G
ENST00000699355.1:c.*381A>G	ENSP00000514328.1:n.*381A>G
ENST00000699356.1:n.2735A>G
ENST00000699357.1:n.2735A>G
ENST00000699358.1:c.2321A>G	ENSP00000514329.1:p.Glu774Gly
ENST00000699360.1:c.2321A>G	ENSP00000514331.1:p.Glu774Gly
ENST00000525621.6:c.2321A>G MANE Select	ENSP00000431885.1:p.Glu774Gly
ENST00000264818.10:c.2321A>G	ENSP00000264818.6:p.Glu774Gly
ENST00000524462.5:c.1766A>G	ENSP00000433203.1:p.Glu589Gly
ENST00000525621.5:c.2321A>G	ENSP00000431885.1:p.Glu774Gly
ENST00000529370.5:c.2321A>G	ENSP00000432728.1:p.Glu774Gly
ENST00000533334.1:c.610A>G
NM_003331.4:c.2321A>G , LRG_121t1:c.2321A>G	NP_003322.3:p.Glu774Gly
XM_011528245.1:c.2321A>G	XP_011526547.1:p.Glu774Gly
XM_011528246.1:c.2024A>G	XP_011526548.1:p.Glu675Gly
XM_011528247.1:c.2024A>G	XP_011526549.1:p.Glu675Gly
XM_011528248.1:c.2321A>G	XP_011526550.1:p.Glu774Gly
XM_011528249.1:c.995A>G	XP_011526551.1:p.Glu332Gly
XM_011528251.1:c.578A>G	XP_011526553.1:p.Glu193Gly
XM_011528246.3:c.2024A>G	XP_011526548.1:p.Glu675Gly
XM_011528249.2:c.995A>G	XP_011526551.1:p.Glu332Gly
XR_001753750.1:n.2478A>G
XR_001753751.1:n.2478A>G
XR_001753752.1:n.2590A>G
XR_002958353.1:n.2359A>G
NM_003331.5:c.2321A>G MANE Select	NP_003322.3:p.Glu774Gly
NM_001385197.1:c.2321A>G	NP_001372126.1:p.Glu774Gly
NM_001385198.1:c.2321A>G	NP_001372127.1:p.Glu774Gly
NM_001385199.1:c.2135A>G	NP_001372128.1:p.Glu712Gly
NM_001385200.1:c.2321A>G	NP_001372129.1:p.Glu774Gly
NM_001385201.1:c.2123A>G	NP_001372130.1:p.Glu708Gly
NM_001385202.1:c.2237A>G	NP_001372131.1:p.Glu746Gly
NM_001385203.1:c.2321A>G	NP_001372132.1:p.Glu774Gly
NM_001385204.1:c.2321A>G	NP_001372133.1:p.Glu774Gly
NM_001385205.1:c.2231A>G	NP_001372134.1:p.Glu744Gly
NM_001385206.1:c.2195A>G	NP_001372135.1:p.Glu732Gly
NM_001385207.1:c.2303A>G	NP_001372136.1:p.Glu768Gly