Canonical Allele Identifier: CA403982893

Gene: TYK2

Linked Data

• gnomAD v4: 19-10352443-G-T
• MyVariant Identifiers: chr19:g.10463119G>T (hg19) ; chr19:g.10352443G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352443G>T , CM000681.2:g.10352443G>T	GRCh38
NC_000019.9:g.10463119G>T , CM000681.1:g.10463119G>T	GRCh37
NC_000019.8:g.10324119G>T	NCBI36
NG_007872.1:g.33130C>A , LRG_121:g.33130C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.*1658C>A	ENSP00000514307.1:n.*1658C>A
ENST00000525976.6:c.3309C>A	ENSP00000434831.2:p.Ser1103Arg
ENST00000527481.3:c.*79C>A	ENSP00000466340.2:n.*79C>A
ENST00000529370.6:n.4685C>A
ENST00000529739.2:n.4118C>A
ENST00000530829.2:c.*2860C>A	ENSP00000436826.2:n.*2860C>A
ENST00000531836.6:c.3309C>A	ENSP00000436175.2:p.Ser1103Arg
ENST00000533334.2:c.*1242+483C>A	ENSP00000432320.2:n.*1242+483C>A
ENST00000534228.2:n.5054+483C>A
ENST00000699354.1:n.1411C>A
ENST00000699355.1:c.*2809C>A	ENSP00000514328.1:n.*2809C>A
ENST00000699356.1:n.4118C>A
ENST00000699357.1:n.5163C>A
ENST00000699358.1:c.3200+483C>A	ENSP00000514329.1:n.3200+483C>A
ENST00000699359.1:c.483C>A
ENST00000699360.1:c.3267C>A	ENSP00000514331.1:p.Ser1089Arg
ENST00000699361.1:n.343C>A
ENST00000699362.1:c.205C>A	ENSP00000514332.1:n.205C>A
ENST00000699363.1:c.205C>A	ENSP00000514333.1:n.205C>A
ENST00000699364.1:n.309C>A
ENST00000699365.1:c.378C>A	ENSP00000514334.1:p.Ser126Arg
ENST00000699366.1:n.111+1371C>A
ENST00000699367.1:n.112-1281C>A
ENST00000699368.1:c.796C>A	ENSP00000514335.1:n.796C>A
ENST00000525621.6:c.3309C>A MANE Select	ENSP00000431885.1:p.Ser1103Arg
ENST00000264818.10:c.3309C>A	ENSP00000264818.6:p.Ser1103Arg
ENST00000524462.5:c.2754C>A	ENSP00000433203.1:p.Ser918Arg
ENST00000525621.5:c.3309C>A	ENSP00000431885.1:p.Ser1103Arg
ENST00000525976.5:c.50C>A
ENST00000527481.2:c.486C>A
ENST00000529422.1:n.116+579C>A
ENST00000529739.1:c.378C>A	ENSP00000436155.1:p.Ser126Arg
ENST00000530220.1:n.331+483C>A
ENST00000530560.5:c.338-1475C>A	ENSP00000465291.1:n.338-1475C>A
ENST00000592137.1:n.463C>A
NM_003331.4:c.3309C>A , LRG_121t1:c.3309C>A	NP_003322.3:p.Ser1103Arg
XM_011528245.1:c.3309C>A	XP_011526547.1:p.Ser1103Arg
XM_011528246.1:c.3012C>A	XP_011526548.1:p.Ser1004Arg
XM_011528247.1:c.3012C>A	XP_011526549.1:p.Ser1004Arg
XM_011528248.1:c.3200+483C>A	XP_011526550.1:n.3200+483C>A
XM_011528249.1:c.1983C>A	XP_011526551.1:p.Ser661Arg
XM_011528251.1:c.1566C>A	XP_011526553.1:p.Ser522Arg
XM_011528246.3:c.3012C>A	XP_011526548.1:p.Ser1004Arg
XM_011528249.2:c.1983C>A	XP_011526551.1:p.Ser661Arg
XR_001753750.1:n.3357+483C>A
XR_001753751.1:n.3861C>A
XR_002958353.1:n.4787C>A
NM_003331.5:c.3309C>A MANE Select	NP_003322.3:p.Ser1103Arg
NM_001385197.1:c.3309C>A	NP_001372126.1:p.Ser1103Arg
NM_001385198.1:c.3168+515C>A	NP_001372127.1:n.3168+515C>A
NM_001385199.1:c.3123C>A	NP_001372128.1:p.Ser1041Arg
NM_001385200.1:c.3306C>A	NP_001372129.1:p.Ser1102Arg
NM_001385201.1:c.3111C>A	NP_001372130.1:p.Ser1037Arg
NM_001385202.1:c.3225C>A	NP_001372131.1:p.Ser1075Arg
NM_001385203.1:c.3390C>A	NP_001372132.1:p.Ser1130Arg
NM_001385204.1:c.3519C>A	NP_001372133.1:p.Ser1173Arg
NM_001385205.1:c.3219C>A	NP_001372134.1:p.Ser1073Arg
NM_001385206.1:c.3183C>A	NP_001372135.1:p.Ser1061Arg
NM_001385207.1:c.3291C>A	NP_001372136.1:p.Ser1097Arg