Canonical Allele Identifier: CA2322388045
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354189C= , CM000681.2:g.10354189C= GRCh38
NC_000019.9:g.10464865C= , CM000681.1:g.10464865C= GRCh37
NC_000019.8:g.10325865C= NCBI36
NG_007872.1:g.31384G= , LRG_121:g.31384G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1110G= ENSP00000514307.1:n.*1110G=
ENST00000525976.6:c.2761G= ENSP00000434831.2:p.Asp921=
ENST00000527481.3:c.2761G= ENSP00000466340.2:p.Asp921=
ENST00000529370.6:n.4137G=
ENST00000529739.2:n.3175G=
ENST00000530829.2:c.*2312G= ENSP00000436826.2:n.*2312G=
ENST00000531836.6:c.2761G= ENSP00000436175.2:p.Asp921=
ENST00000533334.2:c.*803G= ENSP00000432320.2:n.*803G=
ENST00000534228.2:n.4220G=
ENST00000699354.1:n.863G=
ENST00000699355.1:c.*1866G= ENSP00000514328.1:n.*1866G=
ENST00000699356.1:n.3175G=
ENST00000699357.1:n.4220G=
ENST00000699358.1:c.2761G= ENSP00000514329.1:p.Asp921=
ENST00000699360.1:c.2761G= ENSP00000514331.1:p.Asp921=
ENST00000525621.6:c.2761G= MANE Select ENSP00000431885.1:p.Asp921=
ENST00000264818.10:c.2761G= ENSP00000264818.6:p.Asp921=
ENST00000524462.5:c.2206G= ENSP00000433203.1:p.Asp736=
ENST00000525621.5:c.2761G= ENSP00000431885.1:p.Asp921=
ENST00000527481.2:c.57G=
ENST00000529412.1:n.433G=
ENST00000530560.5:c.190G= ENSP00000465291.1:p.Asp64=
NM_003331.4:c.2761G= , LRG_121t1:c.2761G= NP_003322.3:p.Asp921=
XM_011528245.1:c.2761G= XP_011526547.1:p.Asp921=
XM_011528246.1:c.2464G= XP_011526548.1:p.Asp822=
XM_011528247.1:c.2464G= XP_011526549.1:p.Asp822=
XM_011528248.1:c.2761G= XP_011526550.1:p.Asp921=
XM_011528249.1:c.1435G= XP_011526551.1:p.Asp479=
XM_011528251.1:c.1018G= XP_011526553.1:p.Asp340=
XM_011528246.3:c.2464G= XP_011526548.1:p.Asp822=
XM_011528249.2:c.1435G= XP_011526551.1:p.Asp479=
XR_001753750.1:n.2918G=
XR_001753751.1:n.2918G=
XR_002958353.1:n.3844G=
NM_003331.5:c.2761G= MANE Select NP_003322.3:p.Asp921=
NM_001385197.1:c.2761G= NP_001372126.1:p.Asp921=
NM_001385198.1:c.2761G= NP_001372127.1:p.Asp921=
NM_001385199.1:c.2575G= NP_001372128.1:p.Asp859=
NM_001385200.1:c.2758G= NP_001372129.1:p.Asp920=
NM_001385201.1:c.2563G= NP_001372130.1:p.Asp855=
NM_001385202.1:c.2677G= NP_001372131.1:p.Asp893=
NM_001385203.1:c.2842G= NP_001372132.1:p.Asp948=
NM_001385204.1:c.2971G= NP_001372133.1:p.Asp991=
NM_001385205.1:c.2671G= NP_001372134.1:p.Asp891=
NM_001385206.1:c.2635G= NP_001372135.1:p.Asp879=
NM_001385207.1:c.2743G= NP_001372136.1:p.Asp915=