Canonical Allele Identifier: CA403988656

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464846A>C (hg19) ; chr19:g.10354170A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354170A>C , CM000681.2:g.10354170A>C	GRCh38
NC_000019.9:g.10464846A>C , CM000681.1:g.10464846A>C	GRCh37
NC_000019.8:g.10325846A>C	NCBI36
NG_007872.1:g.31403T>G , LRG_121:g.31403T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1129T>G	ENSP00000514307.1:n.*1129T>G
ENST00000525976.6:c.2780T>G	ENSP00000434831.2:p.Val927Gly
ENST00000527481.3:c.2780T>G	ENSP00000466340.2:p.Val927Gly
ENST00000529370.6:n.4156T>G
ENST00000529739.2:n.3194T>G
ENST00000530829.2:c.*2331T>G	ENSP00000436826.2:n.*2331T>G
ENST00000531836.6:c.2780T>G	ENSP00000436175.2:p.Val927Gly
ENST00000533334.2:c.*822T>G	ENSP00000432320.2:n.*822T>G
ENST00000534228.2:n.4239T>G
ENST00000699354.1:n.882T>G
ENST00000699355.1:c.*1885T>G	ENSP00000514328.1:n.*1885T>G
ENST00000699356.1:n.3194T>G
ENST00000699357.1:n.4239T>G
ENST00000699358.1:c.2780T>G	ENSP00000514329.1:p.Val927Gly
ENST00000699360.1:c.2780T>G	ENSP00000514331.1:p.Val927Gly
ENST00000525621.6:c.2780T>G MANE Select	ENSP00000431885.1:p.Val927Gly
ENST00000264818.10:c.2780T>G	ENSP00000264818.6:p.Val927Gly
ENST00000524462.5:c.2225T>G	ENSP00000433203.1:p.Val742Gly
ENST00000525621.5:c.2780T>G	ENSP00000431885.1:p.Val927Gly
ENST00000527481.2:c.76T>G
ENST00000529412.1:n.452T>G
ENST00000530560.5:c.209T>G	ENSP00000465291.1:p.Val70Gly
NM_003331.4:c.2780T>G , LRG_121t1:c.2780T>G	NP_003322.3:p.Val927Gly
XM_011528245.1:c.2780T>G	XP_011526547.1:p.Val927Gly
XM_011528246.1:c.2483T>G	XP_011526548.1:p.Val828Gly
XM_011528247.1:c.2483T>G	XP_011526549.1:p.Val828Gly
XM_011528248.1:c.2780T>G	XP_011526550.1:p.Val927Gly
XM_011528249.1:c.1454T>G	XP_011526551.1:p.Val485Gly
XM_011528251.1:c.1037T>G	XP_011526553.1:p.Val346Gly
XM_011528246.3:c.2483T>G	XP_011526548.1:p.Val828Gly
XM_011528249.2:c.1454T>G	XP_011526551.1:p.Val485Gly
XR_001753750.1:n.2937T>G
XR_001753751.1:n.2937T>G
XR_002958353.1:n.3863T>G
NM_003331.5:c.2780T>G MANE Select	NP_003322.3:p.Val927Gly
NM_001385197.1:c.2780T>G	NP_001372126.1:p.Val927Gly
NM_001385198.1:c.2780T>G	NP_001372127.1:p.Val927Gly
NM_001385199.1:c.2594T>G	NP_001372128.1:p.Val865Gly
NM_001385200.1:c.2777T>G	NP_001372129.1:p.Val926Gly
NM_001385201.1:c.2582T>G	NP_001372130.1:p.Val861Gly
NM_001385202.1:c.2696T>G	NP_001372131.1:p.Val899Gly
NM_001385203.1:c.2861T>G	NP_001372132.1:p.Val954Gly
NM_001385204.1:c.2990T>G	NP_001372133.1:p.Val997Gly
NM_001385205.1:c.2690T>G	NP_001372134.1:p.Val897Gly
NM_001385206.1:c.2654T>G	NP_001372135.1:p.Val885Gly
NM_001385207.1:c.2762T>G	NP_001372136.1:p.Val921Gly