Canonical Allele Identifier: CA631727332

Gene: TYK2

Linked Data

• dbSNP Id: rs35074507
• gnomAD v2: 19-10490181-C-CAATAAATA
• gnomAD v3: 19-10379505-C-CAATAAATA
• gnomAD v4: 19-10379505-C-CAATAAATA
• MyVariant Identifiers: chr19:g.10490197_10490198insAATAAATA (hg19) ; chr19:g.10490181_10490182insAATAAATA (hg19) ; chr19:g.10379521_10379522insAATAAATA (hg38) ; chr19:g.10379505_10379506insAATAAATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10379536_10379543dup , CM000681.2:g.10379536_10379543dup	GRCh38
NC_000019.9:g.10490212_10490219dup , CM000681.1:g.10490212_10490219dup	GRCh37
NC_000019.8:g.10351212_10351219dup	NCBI36
NG_007872.1:g.6060_6067dup , LRG_121:g.6060_6067dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000524470.2:c.-21+102_-21+109dup	ENSP00000514307.1:n.-21+102_-21+109dup
ENST00000525976.6:c.-21+102_-21+109dup	ENSP00000434831.2:n.-21+102_-21+109dup
ENST00000527481.3:c.-21+102_-21+109dup	ENSP00000466340.2:n.-21+102_-21+109dup
ENST00000529370.6:n.311+102_311+109dup
ENST00000529739.2:n.394+102_394+109dup
ENST00000530829.2:c.-21+102_-21+109dup	ENSP00000436826.2:n.-21+102_-21+109dup
ENST00000531836.6:c.-21+102_-21+109dup	ENSP00000436175.2:n.-21+102_-21+109dup
ENST00000533334.2:c.-21+102_-21+109dup	ENSP00000432320.2:n.-21+102_-21+109dup
ENST00000534228.2:n.394+102_394+109dup
ENST00000699355.1:c.-21+102_-21+109dup	ENSP00000514328.1:n.-21+102_-21+109dup
ENST00000699356.1:n.394+102_394+109dup
ENST00000699357.1:n.394+102_394+109dup
ENST00000699358.1:c.-21+102_-21+109dup	ENSP00000514329.1:n.-21+102_-21+109dup
ENST00000699360.1:c.-21+102_-21+109dup	ENSP00000514331.1:n.-21+102_-21+109dup
ENST00000699369.1:n.323+102_323+109dup
ENST00000699370.1:n.345+102_345+109dup
ENST00000699371.1:c.-21+102_-21+109dup	ENSP00000514336.1:n.-21+102_-21+109dup
ENST00000525621.6:c.-21+102_-21+109dup MANE Select	ENSP00000431885.1:n.-21+102_-21+109dup
ENST00000524462.5:c.-91+997_-91+1004dup	ENSP00000433203.1:n.-91+997_-91+1004dup
ENST00000525621.5:c.-21+102_-21+109dup	ENSP00000431885.1:n.-21+102_-21+109dup
ENST00000529370.5:c.-21+102_-21+109dup	ENSP00000432728.1:n.-21+102_-21+109dup
ENST00000530829.1:c.-21+102_-21+109dup	ENSP00000436826.1:n.-21+102_-21+109dup
ENST00000531836.5:c.-21+102_-21+109dup	ENSP00000436175.1:n.-21+102_-21+109dup
NM_003331.4:c.-21+102_-21+109dup , LRG_121t1:c.-21+102_-21+109dup	NP_003322.3:n.-21+102_-21+109dup
XM_011528245.1:c.-21+102_-21+109dup	XP_011526547.1:n.-21+102_-21+109dup
XM_011528248.1:c.-21+102_-21+109dup	XP_011526550.1:n.-21+102_-21+109dup
XM_011528250.1:c.-21+102_-21+109dup	XP_011526552.1:n.-21+102_-21+109dup
XM_011528252.1:c.-21+102_-21+109dup	XP_011526554.1:n.-21+102_-21+109dup
XR_001753750.1:n.137+102_137+109dup
XR_001753751.1:n.137+102_137+109dup
XR_001753752.1:n.137+102_137+109dup
XR_002958353.1:n.137+102_137+109dup
NM_003331.5:c.-21+102_-21+109dup MANE Select	NP_003322.3:n.-21+102_-21+109dup
NM_001385197.1:c.-21+102_-21+109dup	NP_001372126.1:n.-21+102_-21+109dup
NM_001385198.1:c.-21+102_-21+109dup	NP_001372127.1:n.-21+102_-21+109dup
NM_001385199.1:c.-21+102_-21+109dup	NP_001372128.1:n.-21+102_-21+109dup
NM_001385200.1:c.-21+102_-21+109dup	NP_001372129.1:n.-21+102_-21+109dup
NM_001385201.1:c.-21+102_-21+109dup	NP_001372130.1:n.-21+102_-21+109dup
NM_001385202.1:c.-21+102_-21+109dup	NP_001372131.1:n.-21+102_-21+109dup
NM_001385203.1:c.-21+102_-21+109dup	NP_001372132.1:n.-21+102_-21+109dup
NM_001385204.1:c.-21+102_-21+109dup	NP_001372133.1:n.-21+102_-21+109dup
NM_001385205.1:c.-21+102_-21+109dup	NP_001372134.1:n.-21+102_-21+109dup
NM_001385206.1:c.-21+102_-21+109dup	NP_001372135.1:n.-21+102_-21+109dup
NM_001385207.1:c.-21+102_-21+109dup	NP_001372136.1:n.-21+102_-21+109dup