Canonical Allele Identifier: CA403983320

Gene: TYK2

Linked Data

• MyVariant Identifiers: chr19:g.10463210A>T (hg19) ; chr19:g.10352534A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10352534A>T , CM000681.2:g.10352534A>T	GRCh38
NC_000019.9:g.10463210A>T , CM000681.1:g.10463210A>T	GRCh37
NC_000019.8:g.10324210A>T	NCBI36
NG_007872.1:g.33039T>A , LRG_121:g.33039T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524470.2:c.*1567T>A	ENSP00000514307.1:n.*1567T>A
ENST00000525976.6:c.3218T>A	ENSP00000434831.2:p.Leu1073Gln
ENST00000527481.3:c.3099T>A	ENSP00000466340.2:p.Pro1033=
ENST00000529370.6:n.4594T>A
ENST00000529739.2:n.4027T>A
ENST00000530829.2:c.*2769T>A	ENSP00000436826.2:n.*2769T>A
ENST00000531836.6:c.3218T>A	ENSP00000436175.2:p.Leu1073Gln
ENST00000533334.2:c.*1242+392T>A	ENSP00000432320.2:n.*1242+392T>A
ENST00000534228.2:n.5054+392T>A
ENST00000699354.1:n.1320T>A
ENST00000699355.1:c.*2718T>A	ENSP00000514328.1:n.*2718T>A
ENST00000699356.1:n.4027T>A
ENST00000699357.1:n.5072T>A
ENST00000699358.1:c.3200+392T>A	ENSP00000514329.1:n.3200+392T>A
ENST00000699359.1:c.392T>A
ENST00000699360.1:c.3176T>A	ENSP00000514331.1:p.Leu1059Gln
ENST00000699361.1:n.252T>A
ENST00000699362.1:c.114T>A	ENSP00000514332.1:p.Pro38=
ENST00000699363.1:c.114T>A	ENSP00000514333.1:p.Pro38=
ENST00000699364.1:n.218T>A
ENST00000699365.1:c.287T>A	ENSP00000514334.1:p.Leu96Gln
ENST00000699366.1:n.111+1280T>A
ENST00000699367.1:n.111+1280T>A
ENST00000699368.1:c.705T>A	ENSP00000514335.1:n.705T>A
ENST00000525621.6:c.3218T>A MANE Select	ENSP00000431885.1:p.Leu1073Gln
ENST00000264818.10:c.3218T>A	ENSP00000264818.6:p.Leu1073Gln
ENST00000524462.5:c.2663T>A	ENSP00000433203.1:p.Leu888Gln
ENST00000525621.5:c.3218T>A	ENSP00000431885.1:p.Leu1073Gln
ENST00000527481.2:c.395T>A
ENST00000529422.1:n.116+488T>A
ENST00000529739.1:c.287T>A	ENSP00000436155.1:p.Leu96Gln
ENST00000530220.1:n.331+392T>A
ENST00000530560.5:c.337+1508T>A	ENSP00000465291.1:n.337+1508T>A
ENST00000592137.1:n.372T>A
NM_003331.4:c.3218T>A , LRG_121t1:c.3218T>A	NP_003322.3:p.Leu1073Gln
XM_011528245.1:c.3218T>A	XP_011526547.1:p.Leu1073Gln
XM_011528246.1:c.2921T>A	XP_011526548.1:p.Leu974Gln
XM_011528247.1:c.2921T>A	XP_011526549.1:p.Leu974Gln
XM_011528248.1:c.3200+392T>A	XP_011526550.1:n.3200+392T>A
XM_011528249.1:c.1892T>A	XP_011526551.1:p.Leu631Gln
XM_011528251.1:c.1475T>A	XP_011526553.1:p.Leu492Gln
XM_011528246.3:c.2921T>A	XP_011526548.1:p.Leu974Gln
XM_011528249.2:c.1892T>A	XP_011526551.1:p.Leu631Gln
XR_001753750.1:n.3357+392T>A
XR_001753751.1:n.3770T>A
XR_002958353.1:n.4696T>A
NM_003331.5:c.3218T>A MANE Select	NP_003322.3:p.Leu1073Gln
NM_001385197.1:c.3218T>A	NP_001372126.1:p.Leu1073Gln
NM_001385198.1:c.3168+424T>A	NP_001372127.1:n.3168+424T>A
NM_001385199.1:c.3032T>A	NP_001372128.1:p.Leu1011Gln
NM_001385200.1:c.3215T>A	NP_001372129.1:p.Leu1072Gln
NM_001385201.1:c.3020T>A	NP_001372130.1:p.Leu1007Gln
NM_001385202.1:c.3134T>A	NP_001372131.1:p.Leu1045Gln
NM_001385203.1:c.3299T>A	NP_001372132.1:p.Leu1100Gln
NM_001385204.1:c.3428T>A	NP_001372133.1:p.Leu1143Gln
NM_001385205.1:c.3128T>A	NP_001372134.1:p.Leu1043Gln
NM_001385206.1:c.3092T>A	NP_001372135.1:p.Leu1031Gln
NM_001385207.1:c.3200T>A	NP_001372136.1:p.Leu1067Gln