Canonical Allele Identifier: CA2582374517
Gene: TYK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10365640_10365665del , CM000681.2:g.10365640_10365665del GRCh38
NC_000019.9:g.10476316_10476341del , CM000681.1:g.10476316_10476341del GRCh37
NC_000019.8:g.10337316_10337341del NCBI36
NG_007872.1:g.19911_19936del , LRG_121:g.19911_19936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.866_891del ENSP00000514307.1:p.Glu289GlyfsTer9
ENST00000525976.6:c.866_891del ENSP00000434831.2:p.Glu289GlyfsTer9
ENST00000527481.3:c.866_891del ENSP00000466340.2:p.Glu289GlyfsTer9
ENST00000529370.6:n.1197_1222del
ENST00000529739.2:n.1280_1305del
ENST00000530829.2:c.*417_*442del ENSP00000436826.2:n.*417_*442del
ENST00000531836.6:c.866_891del ENSP00000436175.2:p.Glu289GlyfsTer9
ENST00000533334.2:c.866_891del ENSP00000432320.2:p.Glu289GlyfsTer9
ENST00000534228.2:n.1280_1305del
ENST00000699355.1:c.866_891del ENSP00000514328.1:p.Glu289GlyfsTer9
ENST00000699356.1:n.1280_1305del
ENST00000699357.1:n.1280_1305del
ENST00000699358.1:c.866_891del ENSP00000514329.1:p.Glu289GlyfsTer9
ENST00000699360.1:c.866_891del ENSP00000514331.1:p.Glu289GlyfsTer9
ENST00000699369.1:n.1209_1234del
ENST00000699370.1:n.1231_1256del
ENST00000525621.6:c.866_891del MANE Select ENSP00000431885.1:p.Glu289GlyfsTer9
ENST00000264818.10:c.866_891del ENSP00000264818.6:p.Glu289GlyfsTer9
ENST00000524462.5:c.311_336del ENSP00000433203.1:p.Glu104GlyfsTer9
ENST00000525220.1:c.202_227del
ENST00000525621.5:c.866_891del ENSP00000431885.1:p.Glu289GlyfsTer9
ENST00000529370.5:c.866_891del ENSP00000432728.1:p.Glu289GlyfsTer9
NM_003331.4:c.866_891del , LRG_121t1:c.866_891del NP_003322.3:p.Glu289GlyfsTer9
XM_011528245.1:c.866_891del XP_011526547.1:p.Glu289GlyfsTer9
XM_011528246.1:c.569_594del XP_011526548.1:p.Glu190GlyfsTer9
XM_011528247.1:c.569_594del XP_011526549.1:p.Glu190GlyfsTer9
XM_011528248.1:c.866_891del XP_011526550.1:p.Glu289GlyfsTer9
XM_011528250.1:c.866_891del XP_011526552.1:p.Glu289GlyfsTer9
XM_011528252.1:c.866_891del XP_011526554.1:p.Glu289GlyfsTer9
XM_011528246.3:c.569_594del XP_011526548.1:p.Glu190GlyfsTer9
XR_001753750.1:n.1023_1048del
XR_001753751.1:n.1023_1048del
XR_001753752.1:n.1023_1048del
XR_002958353.1:n.1023_1048del
NM_003331.5:c.866_891del MANE Select NP_003322.3:p.Glu289GlyfsTer9
NM_001385197.1:c.866_891del NP_001372126.1:p.Glu289GlyfsTer9
NM_001385198.1:c.866_891del NP_001372127.1:p.Glu289GlyfsTer9
NM_001385199.1:c.866_891del NP_001372128.1:p.Glu289GlyfsTer9
NM_001385200.1:c.866_891del NP_001372129.1:p.Glu289GlyfsTer9
NM_001385201.1:c.866_891del NP_001372130.1:p.Glu289GlyfsTer9
NM_001385202.1:c.866_891del NP_001372131.1:p.Glu289GlyfsTer9
NM_001385203.1:c.866_891del NP_001372132.1:p.Glu289GlyfsTer9
NM_001385204.1:c.866_891del NP_001372133.1:p.Glu289GlyfsTer9
NM_001385205.1:c.776_801del NP_001372134.1:p.Glu259GlyfsTer9
NM_001385206.1:c.866_891del NP_001372135.1:p.Glu289GlyfsTer9
NM_001385207.1:c.866_891del NP_001372136.1:p.Glu289GlyfsTer9