Canonical Allele Identifier: CA403983100

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463137G>T (hg19) ; chr19:g.10352461G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352461G>T , CM000681.2:g.10352461G>T	GRCh38
NC_000019.9:g.10463137G>T , CM000681.1:g.10463137G>T	GRCh37
NC_000019.8:g.10324137G>T	NCBI36
NG_007872.1:g.33112C>A , LRG_121:g.33112C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1640C>A	ENSP00000514307.1:n.*1640C>A
ENST00000525976.6:c.3291C>A	ENSP00000434831.2:p.His1097Gln
ENST00000527481.3:c.*61C>A	ENSP00000466340.2:n.*61C>A
ENST00000529370.6:n.4667C>A
ENST00000529739.2:n.4100C>A
ENST00000530829.2:c.*2842C>A	ENSP00000436826.2:n.*2842C>A
ENST00000531836.6:c.3291C>A	ENSP00000436175.2:p.His1097Gln
ENST00000533334.2:c.*1242+465C>A	ENSP00000432320.2:n.*1242+465C>A
ENST00000534228.2:n.5054+465C>A
ENST00000699354.1:n.1393C>A
ENST00000699355.1:c.*2791C>A	ENSP00000514328.1:n.*2791C>A
ENST00000699356.1:n.4100C>A
ENST00000699357.1:n.5145C>A
ENST00000699358.1:c.3200+465C>A	ENSP00000514329.1:n.3200+465C>A
ENST00000699359.1:c.465C>A
ENST00000699360.1:c.3249C>A	ENSP00000514331.1:p.His1083Gln
ENST00000699361.1:n.325C>A
ENST00000699362.1:c.187C>A	ENSP00000514332.1:n.187C>A
ENST00000699363.1:c.187C>A	ENSP00000514333.1:n.187C>A
ENST00000699364.1:n.291C>A
ENST00000699365.1:c.360C>A	ENSP00000514334.1:p.His120Gln
ENST00000699366.1:n.111+1353C>A
ENST00000699367.1:n.112-1299C>A
ENST00000699368.1:c.778C>A	ENSP00000514335.1:n.778C>A
ENST00000525621.6:c.3291C>A MANE Select	ENSP00000431885.1:p.His1097Gln
ENST00000264818.10:c.3291C>A	ENSP00000264818.6:p.His1097Gln
ENST00000524462.5:c.2736C>A	ENSP00000433203.1:p.His912Gln
ENST00000525621.5:c.3291C>A	ENSP00000431885.1:p.His1097Gln
ENST00000525976.5:c.32C>A
ENST00000527481.2:c.468C>A
ENST00000529422.1:n.116+561C>A
ENST00000529739.1:c.360C>A	ENSP00000436155.1:p.His120Gln
ENST00000530220.1:n.331+465C>A
ENST00000530560.5:c.338-1493C>A	ENSP00000465291.1:n.338-1493C>A
ENST00000592137.1:n.445C>A
NM_003331.4:c.3291C>A , LRG_121t1:c.3291C>A	NP_003322.3:p.His1097Gln
XM_011528245.1:c.3291C>A	XP_011526547.1:p.His1097Gln
XM_011528246.1:c.2994C>A	XP_011526548.1:p.His998Gln
XM_011528247.1:c.2994C>A	XP_011526549.1:p.His998Gln
XM_011528248.1:c.3200+465C>A	XP_011526550.1:n.3200+465C>A
XM_011528249.1:c.1965C>A	XP_011526551.1:p.His655Gln
XM_011528251.1:c.1548C>A	XP_011526553.1:p.His516Gln
XM_011528246.3:c.2994C>A	XP_011526548.1:p.His998Gln
XM_011528249.2:c.1965C>A	XP_011526551.1:p.His655Gln
XR_001753750.1:n.3357+465C>A
XR_001753751.1:n.3843C>A
XR_002958353.1:n.4769C>A
NM_003331.5:c.3291C>A MANE Select	NP_003322.3:p.His1097Gln
NM_001385197.1:c.3291C>A	NP_001372126.1:p.His1097Gln
NM_001385198.1:c.3168+497C>A	NP_001372127.1:n.3168+497C>A
NM_001385199.1:c.3105C>A	NP_001372128.1:p.His1035Gln
NM_001385200.1:c.3288C>A	NP_001372129.1:p.His1096Gln
NM_001385201.1:c.3093C>A	NP_001372130.1:p.His1031Gln
NM_001385202.1:c.3207C>A	NP_001372131.1:p.His1069Gln
NM_001385203.1:c.3372C>A	NP_001372132.1:p.His1124Gln
NM_001385204.1:c.3501C>A	NP_001372133.1:p.His1167Gln
NM_001385205.1:c.3201C>A	NP_001372134.1:p.His1067Gln
NM_001385206.1:c.3165C>A	NP_001372135.1:p.His1055Gln
NM_001385207.1:c.3273C>A	NP_001372136.1:p.His1091Gln