Canonical Allele Identifier: CA2322387149
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10352442G= , CM000681.2:g.10352442G= GRCh38
NC_000019.9:g.10463118G= , CM000681.1:g.10463118G= GRCh37
NC_000019.8:g.10324118G= NCBI36
NG_007872.1:g.33131C= , LRG_121:g.33131C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1659C= ENSP00000514307.1:n.*1659C=
ENST00000525976.6:c.3310C= ENSP00000434831.2:p.Pro1104=
ENST00000527481.3:c.*80C= ENSP00000466340.2:n.*80C=
ENST00000529370.6:n.4686C=
ENST00000529739.2:n.4119C=
ENST00000530829.2:c.*2861C= ENSP00000436826.2:n.*2861C=
ENST00000531836.6:c.3310C= ENSP00000436175.2:p.Pro1104=
ENST00000533334.2:c.*1242+484C= ENSP00000432320.2:n.*1242+484C=
ENST00000534228.2:n.5054+484C=
ENST00000699354.1:n.1412C=
ENST00000699355.1:c.*2810C= ENSP00000514328.1:n.*2810C=
ENST00000699356.1:n.4119C=
ENST00000699357.1:n.5164C=
ENST00000699358.1:c.3200+484C= ENSP00000514329.1:n.3200+484C=
ENST00000699359.1:c.484C=
ENST00000699360.1:c.3268C= ENSP00000514331.1:p.Pro1090=
ENST00000699361.1:n.344C=
ENST00000699362.1:c.206C= ENSP00000514332.1:n.206C=
ENST00000699363.1:c.206C= ENSP00000514333.1:n.206C=
ENST00000699364.1:n.310C=
ENST00000699365.1:c.379C= ENSP00000514334.1:p.Pro127=
ENST00000699366.1:n.111+1372C=
ENST00000699367.1:n.112-1280C=
ENST00000699368.1:c.797C= ENSP00000514335.1:n.797C=
ENST00000525621.6:c.3310C= MANE Select ENSP00000431885.1:p.Pro1104=
ENST00000264818.10:c.3310C= ENSP00000264818.6:p.Pro1104=
ENST00000524462.5:c.2755C= ENSP00000433203.1:p.Pro919=
ENST00000525621.5:c.3310C= ENSP00000431885.1:p.Pro1104=
ENST00000525976.5:c.51C=
ENST00000527481.2:c.487C=
ENST00000529422.1:n.116+580C=
ENST00000529739.1:c.379C= ENSP00000436155.1:p.Pro127=
ENST00000530220.1:n.331+484C=
ENST00000530560.5:c.338-1474C= ENSP00000465291.1:n.338-1474C=
ENST00000592137.1:n.464C=
NM_003331.4:c.3310C= , LRG_121t1:c.3310C= NP_003322.3:p.Pro1104=
XM_011528245.1:c.3310C= XP_011526547.1:p.Pro1104=
XM_011528246.1:c.3013C= XP_011526548.1:p.Pro1005=
XM_011528247.1:c.3013C= XP_011526549.1:p.Pro1005=
XM_011528248.1:c.3200+484C= XP_011526550.1:n.3200+484C=
XM_011528249.1:c.1984C= XP_011526551.1:p.Pro662=
XM_011528251.1:c.1567C= XP_011526553.1:p.Pro523=
XM_011528246.3:c.3013C= XP_011526548.1:p.Pro1005=
XM_011528249.2:c.1984C= XP_011526551.1:p.Pro662=
XR_001753750.1:n.3357+484C=
XR_001753751.1:n.3862C=
XR_002958353.1:n.4788C=
NM_003331.5:c.3310C= MANE Select NP_003322.3:p.Pro1104=
NM_001385197.1:c.3310C= NP_001372126.1:p.Pro1104=
NM_001385198.1:c.3168+516C= NP_001372127.1:n.3168+516C=
NM_001385199.1:c.3124C= NP_001372128.1:p.Pro1042=
NM_001385200.1:c.3307C= NP_001372129.1:p.Pro1103=
NM_001385201.1:c.3112C= NP_001372130.1:p.Pro1038=
NM_001385202.1:c.3226C= NP_001372131.1:p.Pro1076=
NM_001385203.1:c.3391C= NP_001372132.1:p.Pro1131=
NM_001385204.1:c.3520C= NP_001372133.1:p.Pro1174=
NM_001385205.1:c.3220C= NP_001372134.1:p.Pro1074=
NM_001385206.1:c.3184C= NP_001372135.1:p.Pro1062=
NM_001385207.1:c.3292C= NP_001372136.1:p.Pro1098=