Canonical Allele Identifier: CA2322387990
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354077T= , CM000681.2:g.10354077T= GRCh38
NC_000019.9:g.10464753T= , CM000681.1:g.10464753T= GRCh37
NC_000019.8:g.10325753T= NCBI36
NG_007872.1:g.31496A= , LRG_121:g.31496A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1222A= ENSP00000514307.1:n.*1222A=
ENST00000525976.6:c.2873A= ENSP00000434831.2:p.His958=
ENST00000527481.3:c.2873A= ENSP00000466340.2:p.His958=
ENST00000529370.6:n.4249A=
ENST00000529739.2:n.3287A=
ENST00000530829.2:c.*2424A= ENSP00000436826.2:n.*2424A=
ENST00000531836.6:c.2873A= ENSP00000436175.2:p.His958=
ENST00000533334.2:c.*915A= ENSP00000432320.2:n.*915A=
ENST00000534228.2:n.4332A=
ENST00000699354.1:n.975A=
ENST00000699355.1:c.*1978A= ENSP00000514328.1:n.*1978A=
ENST00000699356.1:n.3287A=
ENST00000699357.1:n.4332A=
ENST00000699358.1:c.2873A= ENSP00000514329.1:p.His958=
ENST00000699359.1:c.79A=
ENST00000699360.1:c.2873A= ENSP00000514331.1:p.His958=
ENST00000699368.1:c.77A= ENSP00000514335.1:p.His26=
ENST00000525621.6:c.2873A= MANE Select ENSP00000431885.1:p.His958=
ENST00000264818.10:c.2873A= ENSP00000264818.6:p.His958=
ENST00000524462.5:c.2318A= ENSP00000433203.1:p.His773=
ENST00000525621.5:c.2873A= ENSP00000431885.1:p.His958=
ENST00000527481.2:c.169A=
ENST00000529412.1:n.545A=
ENST00000529739.1:c.-454A= ENSP00000436155.1:n.-454A=
ENST00000530560.5:c.302A= ENSP00000465291.1:p.His101=
ENST00000592137.1:n.27A=
NM_003331.4:c.2873A= , LRG_121t1:c.2873A= NP_003322.3:p.His958=
XM_011528245.1:c.2873A= XP_011526547.1:p.His958=
XM_011528246.1:c.2576A= XP_011526548.1:p.His859=
XM_011528247.1:c.2576A= XP_011526549.1:p.His859=
XM_011528248.1:c.2873A= XP_011526550.1:p.His958=
XM_011528249.1:c.1547A= XP_011526551.1:p.His516=
XM_011528251.1:c.1130A= XP_011526553.1:p.His377=
XM_011528246.3:c.2576A= XP_011526548.1:p.His859=
XM_011528249.2:c.1547A= XP_011526551.1:p.His516=
XR_001753750.1:n.3030A=
XR_001753751.1:n.3030A=
XR_002958353.1:n.3956A=
NM_003331.5:c.2873A= MANE Select NP_003322.3:p.His958=
NM_001385197.1:c.2873A= NP_001372126.1:p.His958=
NM_001385198.1:c.2873A= NP_001372127.1:p.His958=
NM_001385199.1:c.2687A= NP_001372128.1:p.His896=
NM_001385200.1:c.2870A= NP_001372129.1:p.His957=
NM_001385201.1:c.2675A= NP_001372130.1:p.His892=
NM_001385202.1:c.2789A= NP_001372131.1:p.His930=
NM_001385203.1:c.2954A= NP_001372132.1:p.His985=
NM_001385204.1:c.3083A= NP_001372133.1:p.His1028=
NM_001385205.1:c.2783A= NP_001372134.1:p.His928=
NM_001385206.1:c.2747A= NP_001372135.1:p.His916=
NM_001385207.1:c.2855A= NP_001372136.1:p.His952=