Canonical Allele Identifier: CA403987616

Gene: TYK2

Linked Data

• ClinVar Variation Id: 1376443
• ClinVar RCV Id: RCV001912009
• dbSNP Id: rs2036762184
• MyVariant Identifiers: chr19:g.10464726T>C (hg19) ; chr19:g.10354050T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354050T>C , CM000681.2:g.10354050T>C	GRCh38
NC_000019.9:g.10464726T>C , CM000681.1:g.10464726T>C	GRCh37
NC_000019.8:g.10325726T>C	NCBI36
NG_007872.1:g.31523A>G , LRG_121:g.31523A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1249A>G	ENSP00000514307.1:n.*1249A>G
ENST00000525976.6:c.2900A>G	ENSP00000434831.2:p.Glu967Gly
ENST00000527481.3:c.2900A>G	ENSP00000466340.2:p.Glu967Gly
ENST00000529370.6:n.4276A>G
ENST00000529739.2:n.3314A>G
ENST00000530829.2:c.*2451A>G	ENSP00000436826.2:n.*2451A>G
ENST00000531836.6:c.2900A>G	ENSP00000436175.2:p.Glu967Gly
ENST00000533334.2:c.*942A>G	ENSP00000432320.2:n.*942A>G
ENST00000534228.2:n.4359A>G
ENST00000699354.1:n.1002A>G
ENST00000699355.1:c.*2005A>G	ENSP00000514328.1:n.*2005A>G
ENST00000699356.1:n.3314A>G
ENST00000699357.1:n.4359A>G
ENST00000699358.1:c.2900A>G	ENSP00000514329.1:p.Glu967Gly
ENST00000699359.1:c.106A>G
ENST00000699360.1:c.2900A>G	ENSP00000514331.1:p.Glu967Gly
ENST00000699368.1:c.104A>G	ENSP00000514335.1:p.Glu35Gly
ENST00000525621.6:c.2900A>G MANE Select	ENSP00000431885.1:p.Glu967Gly
ENST00000264818.10:c.2900A>G	ENSP00000264818.6:p.Glu967Gly
ENST00000524462.5:c.2345A>G	ENSP00000433203.1:p.Glu782Gly
ENST00000525621.5:c.2900A>G	ENSP00000431885.1:p.Glu967Gly
ENST00000527481.2:c.196A>G
ENST00000529412.1:n.572A>G
ENST00000529739.1:c.-427A>G	ENSP00000436155.1:n.-427A>G
ENST00000530560.5:c.329A>G	ENSP00000465291.1:p.Glu110Gly
ENST00000592137.1:n.54A>G
NM_003331.4:c.2900A>G , LRG_121t1:c.2900A>G	NP_003322.3:p.Glu967Gly
XM_011528245.1:c.2900A>G	XP_011526547.1:p.Glu967Gly
XM_011528246.1:c.2603A>G	XP_011526548.1:p.Glu868Gly
XM_011528247.1:c.2603A>G	XP_011526549.1:p.Glu868Gly
XM_011528248.1:c.2900A>G	XP_011526550.1:p.Glu967Gly
XM_011528249.1:c.1574A>G	XP_011526551.1:p.Glu525Gly
XM_011528251.1:c.1157A>G	XP_011526553.1:p.Glu386Gly
XM_011528246.3:c.2603A>G	XP_011526548.1:p.Glu868Gly
XM_011528249.2:c.1574A>G	XP_011526551.1:p.Glu525Gly
XR_001753750.1:n.3057A>G
XR_001753751.1:n.3057A>G
XR_002958353.1:n.3983A>G
NM_003331.5:c.2900A>G MANE Select	NP_003322.3:p.Glu967Gly
NM_001385197.1:c.2900A>G	NP_001372126.1:p.Glu967Gly
NM_001385198.1:c.2900A>G	NP_001372127.1:p.Glu967Gly
NM_001385199.1:c.2714A>G	NP_001372128.1:p.Glu905Gly
NM_001385200.1:c.2897A>G	NP_001372129.1:p.Glu966Gly
NM_001385201.1:c.2702A>G	NP_001372130.1:p.Glu901Gly
NM_001385202.1:c.2816A>G	NP_001372131.1:p.Glu939Gly
NM_001385203.1:c.2981A>G	NP_001372132.1:p.Glu994Gly
NM_001385204.1:c.3110A>G	NP_001372133.1:p.Glu1037Gly
NM_001385205.1:c.2810A>G	NP_001372134.1:p.Glu937Gly
NM_001385206.1:c.2774A>G	NP_001372135.1:p.Glu925Gly
NM_001385207.1:c.2882A>G	NP_001372136.1:p.Glu961Gly