Canonical Allele Identifier: CA2582375172
Gene: TYK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10368812_10368813insT , CM000681.2:g.10368812_10368813insT GRCh38
NC_000019.9:g.10479488_10479489insT , CM000681.1:g.10479488_10479489insT GRCh37
NC_000019.8:g.10340488_10340489insT NCBI36
NG_007872.1:g.16760_16761insA , LRG_121:g.16760_16761insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.194-395_194-394insA ENSP00000514307.1:n.194-395_194-394insA
ENST00000525976.6:c.194-395_194-394insA ENSP00000434831.2:n.194-395_194-394insA
ENST00000527481.3:c.194-395_194-394insA ENSP00000466340.2:n.194-395_194-394insA
ENST00000529370.6:n.525-395_525-394insA
ENST00000529739.2:n.608-395_608-394insA
ENST00000530829.2:c.315-395_315-394insA ENSP00000436826.2:n.315-395_315-394insA
ENST00000531836.6:c.194-395_194-394insA ENSP00000436175.2:n.194-395_194-394insA
ENST00000533334.2:c.194-395_194-394insA ENSP00000432320.2:n.194-395_194-394insA
ENST00000534228.2:n.608-395_608-394insA
ENST00000699355.1:c.194-395_194-394insA ENSP00000514328.1:n.194-395_194-394insA
ENST00000699356.1:n.608-395_608-394insA
ENST00000699357.1:n.608-395_608-394insA
ENST00000699358.1:c.194-395_194-394insA ENSP00000514329.1:n.194-395_194-394insA
ENST00000699360.1:c.194-395_194-394insA ENSP00000514331.1:n.194-395_194-394insA
ENST00000699369.1:n.537-395_537-394insA
ENST00000699370.1:n.559-395_559-394insA
ENST00000699371.1:c.194-395_194-394insA ENSP00000514336.1:n.194-395_194-394insA
ENST00000525621.6:c.194-395_194-394insA MANE Select ENSP00000431885.1:n.194-395_194-394insA
ENST00000264818.10:c.194-395_194-394insA ENSP00000264818.6:n.194-395_194-394insA
ENST00000524462.5:c.-90-2233_-90-2232insA ENSP00000433203.1:n.-90-2233_-90-2232insA
ENST00000525621.5:c.194-395_194-394insA ENSP00000431885.1:n.194-395_194-394insA
ENST00000529370.5:c.194-395_194-394insA ENSP00000432728.1:n.194-395_194-394insA
ENST00000530829.1:c.315-395_315-394insA ENSP00000436826.1:n.315-395_315-394insA
ENST00000531836.5:c.194-395_194-394insA ENSP00000436175.1:n.194-395_194-394insA
NM_003331.4:c.194-395_194-394insA , LRG_121t1:c.194-395_194-394insA NP_003322.3:n.194-395_194-394insA
XM_011528245.1:c.194-395_194-394insA XP_011526547.1:n.194-395_194-394insA
XM_011528246.1:c.-336-50_-336-49insA XP_011526548.1:n.-336-50_-336-49insA
XM_011528247.1:c.-104-395_-104-394insA XP_011526549.1:n.-104-395_-104-394insA
XM_011528248.1:c.194-395_194-394insA XP_011526550.1:n.194-395_194-394insA
XM_011528250.1:c.194-395_194-394insA XP_011526552.1:n.194-395_194-394insA
XM_011528252.1:c.194-395_194-394insA XP_011526554.1:n.194-395_194-394insA
XM_011528246.3:c.-336-50_-336-49insA XP_011526548.1:n.-336-50_-336-49insA
XR_001753750.1:n.351-395_351-394insA
XR_001753751.1:n.351-395_351-394insA
XR_001753752.1:n.351-395_351-394insA
XR_002958353.1:n.351-395_351-394insA
NM_003331.5:c.194-395_194-394insA MANE Select NP_003322.3:n.194-395_194-394insA
NM_001385197.1:c.194-395_194-394insA NP_001372126.1:n.194-395_194-394insA
NM_001385198.1:c.194-395_194-394insA NP_001372127.1:n.194-395_194-394insA
NM_001385199.1:c.194-395_194-394insA NP_001372128.1:n.194-395_194-394insA
NM_001385200.1:c.194-395_194-394insA NP_001372129.1:n.194-395_194-394insA
NM_001385201.1:c.194-395_194-394insA NP_001372130.1:n.194-395_194-394insA
NM_001385202.1:c.194-395_194-394insA NP_001372131.1:n.194-395_194-394insA
NM_001385203.1:c.194-395_194-394insA NP_001372132.1:n.194-395_194-394insA
NM_001385204.1:c.194-395_194-394insA NP_001372133.1:n.194-395_194-394insA
NM_001385205.1:c.194-395_194-394insA NP_001372134.1:n.194-395_194-394insA
NM_001385206.1:c.194-395_194-394insA NP_001372135.1:n.194-395_194-394insA
NM_001385207.1:c.194-395_194-394insA NP_001372136.1:n.194-395_194-394insA