Canonical Allele Identifier: CA403988210

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10464796A>C (hg19) ; chr19:g.10354120A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10354120A>C , CM000681.2:g.10354120A>C	GRCh38
NC_000019.9:g.10464796A>C , CM000681.1:g.10464796A>C	GRCh37
NC_000019.8:g.10325796A>C	NCBI36
NG_007872.1:g.31453T>G , LRG_121:g.31453T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1179T>G	ENSP00000514307.1:n.*1179T>G
ENST00000525976.6:c.2830T>G	ENSP00000434831.2:p.Trp944Gly
ENST00000527481.3:c.2830T>G	ENSP00000466340.2:p.Trp944Gly
ENST00000529370.6:n.4206T>G
ENST00000529739.2:n.3244T>G
ENST00000530829.2:c.*2381T>G	ENSP00000436826.2:n.*2381T>G
ENST00000531836.6:c.2830T>G	ENSP00000436175.2:p.Trp944Gly
ENST00000533334.2:c.*872T>G	ENSP00000432320.2:n.*872T>G
ENST00000534228.2:n.4289T>G
ENST00000699354.1:n.932T>G
ENST00000699355.1:c.*1935T>G	ENSP00000514328.1:n.*1935T>G
ENST00000699356.1:n.3244T>G
ENST00000699357.1:n.4289T>G
ENST00000699358.1:c.2830T>G	ENSP00000514329.1:p.Trp944Gly
ENST00000699359.1:c.36T>G
ENST00000699360.1:c.2830T>G	ENSP00000514331.1:p.Trp944Gly
ENST00000699368.1:c.34T>G	ENSP00000514335.1:p.Trp12Gly
ENST00000525621.6:c.2830T>G MANE Select	ENSP00000431885.1:p.Trp944Gly
ENST00000264818.10:c.2830T>G	ENSP00000264818.6:p.Trp944Gly
ENST00000524462.5:c.2275T>G	ENSP00000433203.1:p.Trp759Gly
ENST00000525621.5:c.2830T>G	ENSP00000431885.1:p.Trp944Gly
ENST00000527481.2:c.126T>G
ENST00000529412.1:n.502T>G
ENST00000530560.5:c.259T>G	ENSP00000465291.1:p.Trp87Gly
NM_003331.4:c.2830T>G , LRG_121t1:c.2830T>G	NP_003322.3:p.Trp944Gly
XM_011528245.1:c.2830T>G	XP_011526547.1:p.Trp944Gly
XM_011528246.1:c.2533T>G	XP_011526548.1:p.Trp845Gly
XM_011528247.1:c.2533T>G	XP_011526549.1:p.Trp845Gly
XM_011528248.1:c.2830T>G	XP_011526550.1:p.Trp944Gly
XM_011528249.1:c.1504T>G	XP_011526551.1:p.Trp502Gly
XM_011528251.1:c.1087T>G	XP_011526553.1:p.Trp363Gly
XM_011528246.3:c.2533T>G	XP_011526548.1:p.Trp845Gly
XM_011528249.2:c.1504T>G	XP_011526551.1:p.Trp502Gly
XR_001753750.1:n.2987T>G
XR_001753751.1:n.2987T>G
XR_002958353.1:n.3913T>G
NM_003331.5:c.2830T>G MANE Select	NP_003322.3:p.Trp944Gly
NM_001385197.1:c.2830T>G	NP_001372126.1:p.Trp944Gly
NM_001385198.1:c.2830T>G	NP_001372127.1:p.Trp944Gly
NM_001385199.1:c.2644T>G	NP_001372128.1:p.Trp882Gly
NM_001385200.1:c.2827T>G	NP_001372129.1:p.Trp943Gly
NM_001385201.1:c.2632T>G	NP_001372130.1:p.Trp878Gly
NM_001385202.1:c.2746T>G	NP_001372131.1:p.Trp916Gly
NM_001385203.1:c.2911T>G	NP_001372132.1:p.Trp971Gly
NM_001385204.1:c.3040T>G	NP_001372133.1:p.Trp1014Gly
NM_001385205.1:c.2740T>G	NP_001372134.1:p.Trp914Gly
NM_001385206.1:c.2704T>G	NP_001372135.1:p.Trp902Gly
NM_001385207.1:c.2812T>G	NP_001372136.1:p.Trp938Gly