Canonical Allele Identifier: CA505371272

Gene: TYK2

Linked Data

• dbSNP Id: rs2040861756
• gnomAD v3: 19-10352494-G-T
• gnomAD v4: 19-10352494-G-T
• MyVariant Identifiers: chr19:g.10463170G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352494G>T , CM000681.2:g.10352494G>T	GRCh38
NC_000019.9:g.10463170G>T , CM000681.1:g.10463170G>T	GRCh37
NC_000019.8:g.10324170G>T	NCBI36
NG_007872.1:g.33079C>A , LRG_121:g.33079C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1607C>A	ENSP00000514307.1:n.*1607C>A
ENST00000525976.6:c.3258C>A	ENSP00000434831.2:p.Ser1086=
ENST00000527481.3:c.*28C>A	ENSP00000466340.2:n.*28C>A
ENST00000529370.6:n.4634C>A
ENST00000529739.2:n.4067C>A
ENST00000530829.2:c.*2809C>A	ENSP00000436826.2:n.*2809C>A
ENST00000531836.6:c.3258C>A	ENSP00000436175.2:p.Ser1086=
ENST00000533334.2:c.*1242+432C>A	ENSP00000432320.2:n.*1242+432C>A
ENST00000534228.2:n.5054+432C>A
ENST00000699354.1:n.1360C>A
ENST00000699355.1:c.*2758C>A	ENSP00000514328.1:n.*2758C>A
ENST00000699356.1:n.4067C>A
ENST00000699357.1:n.5112C>A
ENST00000699358.1:c.3200+432C>A	ENSP00000514329.1:n.3200+432C>A
ENST00000699359.1:c.432C>A
ENST00000699360.1:c.3216C>A	ENSP00000514331.1:p.Ser1072=
ENST00000699361.1:n.292C>A
ENST00000699362.1:c.154C>A	ENSP00000514332.1:n.154C>A
ENST00000699363.1:c.154C>A	ENSP00000514333.1:n.154C>A
ENST00000699364.1:n.258C>A
ENST00000699365.1:c.327C>A	ENSP00000514334.1:p.Ser109=
ENST00000699366.1:n.111+1320C>A
ENST00000699367.1:n.111+1320C>A
ENST00000699368.1:c.745C>A	ENSP00000514335.1:n.745C>A
ENST00000525621.6:c.3258C>A MANE Select	ENSP00000431885.1:p.Ser1086=
ENST00000264818.10:c.3258C>A	ENSP00000264818.6:p.Ser1086=
ENST00000524462.5:c.2703C>A	ENSP00000433203.1:p.Ser901=
ENST00000525621.5:c.3258C>A	ENSP00000431885.1:p.Ser1086=
ENST00000527481.2:c.435C>A
ENST00000529422.1:n.116+528C>A
ENST00000529739.1:c.327C>A	ENSP00000436155.1:p.Ser109=
ENST00000530220.1:n.331+432C>A
ENST00000530560.5:c.338-1526C>A	ENSP00000465291.1:n.338-1526C>A
ENST00000592137.1:n.412C>A
NM_003331.4:c.3258C>A , LRG_121t1:c.3258C>A	NP_003322.3:p.Ser1086=
XM_011528245.1:c.3258C>A	XP_011526547.1:p.Ser1086=
XM_011528246.1:c.2961C>A	XP_011526548.1:p.Ser987=
XM_011528247.1:c.2961C>A	XP_011526549.1:p.Ser987=
XM_011528248.1:c.3200+432C>A	XP_011526550.1:n.3200+432C>A
XM_011528249.1:c.1932C>A	XP_011526551.1:p.Ser644=
XM_011528251.1:c.1515C>A	XP_011526553.1:p.Ser505=
XM_011528246.3:c.2961C>A	XP_011526548.1:p.Ser987=
XM_011528249.2:c.1932C>A	XP_011526551.1:p.Ser644=
XR_001753750.1:n.3357+432C>A
XR_001753751.1:n.3810C>A
XR_002958353.1:n.4736C>A
NM_003331.5:c.3258C>A MANE Select	NP_003322.3:p.Ser1086=
NM_001385197.1:c.3258C>A	NP_001372126.1:p.Ser1086=
NM_001385198.1:c.3168+464C>A	NP_001372127.1:n.3168+464C>A
NM_001385199.1:c.3072C>A	NP_001372128.1:p.Ser1024=
NM_001385200.1:c.3255C>A	NP_001372129.1:p.Ser1085=
NM_001385201.1:c.3060C>A	NP_001372130.1:p.Ser1020=
NM_001385202.1:c.3174C>A	NP_001372131.1:p.Ser1058=
NM_001385203.1:c.3339C>A	NP_001372132.1:p.Ser1113=
NM_001385204.1:c.3468C>A	NP_001372133.1:p.Ser1156=
NM_001385205.1:c.3168C>A	NP_001372134.1:p.Ser1056=
NM_001385206.1:c.3132C>A	NP_001372135.1:p.Ser1044=
NM_001385207.1:c.3240C>A	NP_001372136.1:p.Ser1080=