Canonical Allele Identifier: CA403983173

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463150T>C (hg19) ; chr19:g.10352474T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352474T>C , CM000681.2:g.10352474T>C	GRCh38
NC_000019.9:g.10463150T>C , CM000681.1:g.10463150T>C	GRCh37
NC_000019.8:g.10324150T>C	NCBI36
NG_007872.1:g.33099A>G , LRG_121:g.33099A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1627A>G	ENSP00000514307.1:n.*1627A>G
ENST00000525976.6:c.3278A>G	ENSP00000434831.2:p.Glu1093Gly
ENST00000527481.3:c.*48A>G	ENSP00000466340.2:n.*48A>G
ENST00000529370.6:n.4654A>G
ENST00000529739.2:n.4087A>G
ENST00000530829.2:c.*2829A>G	ENSP00000436826.2:n.*2829A>G
ENST00000531836.6:c.3278A>G	ENSP00000436175.2:p.Glu1093Gly
ENST00000533334.2:c.*1242+452A>G	ENSP00000432320.2:n.*1242+452A>G
ENST00000534228.2:n.5054+452A>G
ENST00000699354.1:n.1380A>G
ENST00000699355.1:c.*2778A>G	ENSP00000514328.1:n.*2778A>G
ENST00000699356.1:n.4087A>G
ENST00000699357.1:n.5132A>G
ENST00000699358.1:c.3200+452A>G	ENSP00000514329.1:n.3200+452A>G
ENST00000699359.1:c.452A>G
ENST00000699360.1:c.3236A>G	ENSP00000514331.1:p.Glu1079Gly
ENST00000699361.1:n.312A>G
ENST00000699362.1:c.174A>G	ENSP00000514332.1:n.174A>G
ENST00000699363.1:c.174A>G	ENSP00000514333.1:n.174A>G
ENST00000699364.1:n.278A>G
ENST00000699365.1:c.347A>G	ENSP00000514334.1:p.Glu116Gly
ENST00000699366.1:n.111+1340A>G
ENST00000699367.1:n.112-1312A>G
ENST00000699368.1:c.765A>G	ENSP00000514335.1:n.765A>G
ENST00000525621.6:c.3278A>G MANE Select	ENSP00000431885.1:p.Glu1093Gly
ENST00000264818.10:c.3278A>G	ENSP00000264818.6:p.Glu1093Gly
ENST00000524462.5:c.2723A>G	ENSP00000433203.1:p.Glu908Gly
ENST00000525621.5:c.3278A>G	ENSP00000431885.1:p.Glu1093Gly
ENST00000525976.5:c.19A>G
ENST00000527481.2:c.455A>G
ENST00000529422.1:n.116+548A>G
ENST00000529739.1:c.347A>G	ENSP00000436155.1:p.Glu116Gly
ENST00000530220.1:n.331+452A>G
ENST00000530560.5:c.338-1506A>G	ENSP00000465291.1:n.338-1506A>G
ENST00000592137.1:n.432A>G
NM_003331.4:c.3278A>G , LRG_121t1:c.3278A>G	NP_003322.3:p.Glu1093Gly
XM_011528245.1:c.3278A>G	XP_011526547.1:p.Glu1093Gly
XM_011528246.1:c.2981A>G	XP_011526548.1:p.Glu994Gly
XM_011528247.1:c.2981A>G	XP_011526549.1:p.Glu994Gly
XM_011528248.1:c.3200+452A>G	XP_011526550.1:n.3200+452A>G
XM_011528249.1:c.1952A>G	XP_011526551.1:p.Glu651Gly
XM_011528251.1:c.1535A>G	XP_011526553.1:p.Glu512Gly
XM_011528246.3:c.2981A>G	XP_011526548.1:p.Glu994Gly
XM_011528249.2:c.1952A>G	XP_011526551.1:p.Glu651Gly
XR_001753750.1:n.3357+452A>G
XR_001753751.1:n.3830A>G
XR_002958353.1:n.4756A>G
NM_003331.5:c.3278A>G MANE Select	NP_003322.3:p.Glu1093Gly
NM_001385197.1:c.3278A>G	NP_001372126.1:p.Glu1093Gly
NM_001385198.1:c.3168+484A>G	NP_001372127.1:n.3168+484A>G
NM_001385199.1:c.3092A>G	NP_001372128.1:p.Glu1031Gly
NM_001385200.1:c.3275A>G	NP_001372129.1:p.Glu1092Gly
NM_001385201.1:c.3080A>G	NP_001372130.1:p.Glu1027Gly
NM_001385202.1:c.3194A>G	NP_001372131.1:p.Glu1065Gly
NM_001385203.1:c.3359A>G	NP_001372132.1:p.Glu1120Gly
NM_001385204.1:c.3488A>G	NP_001372133.1:p.Glu1163Gly
NM_001385205.1:c.3188A>G	NP_001372134.1:p.Glu1063Gly
NM_001385206.1:c.3152A>G	NP_001372135.1:p.Glu1051Gly
NM_001385207.1:c.3260A>G	NP_001372136.1:p.Glu1087Gly