Canonical Allele Identifier: CA2322388037
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354172C= , CM000681.2:g.10354172C= GRCh38
NC_000019.9:g.10464848C= , CM000681.1:g.10464848C= GRCh37
NC_000019.8:g.10325848C= NCBI36
NG_007872.1:g.31401G= , LRG_121:g.31401G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1127G= ENSP00000514307.1:n.*1127G=
ENST00000525976.6:c.2778G= ENSP00000434831.2:p.Met926=
ENST00000527481.3:c.2778G= ENSP00000466340.2:p.Met926=
ENST00000529370.6:n.4154G=
ENST00000529739.2:n.3192G=
ENST00000530829.2:c.*2329G= ENSP00000436826.2:n.*2329G=
ENST00000531836.6:c.2778G= ENSP00000436175.2:p.Met926=
ENST00000533334.2:c.*820G= ENSP00000432320.2:n.*820G=
ENST00000534228.2:n.4237G=
ENST00000699354.1:n.880G=
ENST00000699355.1:c.*1883G= ENSP00000514328.1:n.*1883G=
ENST00000699356.1:n.3192G=
ENST00000699357.1:n.4237G=
ENST00000699358.1:c.2778G= ENSP00000514329.1:p.Met926=
ENST00000699360.1:c.2778G= ENSP00000514331.1:p.Met926=
ENST00000525621.6:c.2778G= MANE Select ENSP00000431885.1:p.Met926=
ENST00000264818.10:c.2778G= ENSP00000264818.6:p.Met926=
ENST00000524462.5:c.2223G= ENSP00000433203.1:p.Met741=
ENST00000525621.5:c.2778G= ENSP00000431885.1:p.Met926=
ENST00000527481.2:c.74G=
ENST00000529412.1:n.450G=
ENST00000530560.5:c.207G= ENSP00000465291.1:p.Met69=
NM_003331.4:c.2778G= , LRG_121t1:c.2778G= NP_003322.3:p.Met926=
XM_011528245.1:c.2778G= XP_011526547.1:p.Met926=
XM_011528246.1:c.2481G= XP_011526548.1:p.Met827=
XM_011528247.1:c.2481G= XP_011526549.1:p.Met827=
XM_011528248.1:c.2778G= XP_011526550.1:p.Met926=
XM_011528249.1:c.1452G= XP_011526551.1:p.Met484=
XM_011528251.1:c.1035G= XP_011526553.1:p.Met345=
XM_011528246.3:c.2481G= XP_011526548.1:p.Met827=
XM_011528249.2:c.1452G= XP_011526551.1:p.Met484=
XR_001753750.1:n.2935G=
XR_001753751.1:n.2935G=
XR_002958353.1:n.3861G=
NM_003331.5:c.2778G= MANE Select NP_003322.3:p.Met926=
NM_001385197.1:c.2778G= NP_001372126.1:p.Met926=
NM_001385198.1:c.2778G= NP_001372127.1:p.Met926=
NM_001385199.1:c.2592G= NP_001372128.1:p.Met864=
NM_001385200.1:c.2775G= NP_001372129.1:p.Met925=
NM_001385201.1:c.2580G= NP_001372130.1:p.Met860=
NM_001385202.1:c.2694G= NP_001372131.1:p.Met898=
NM_001385203.1:c.2859G= NP_001372132.1:p.Met953=
NM_001385204.1:c.2988G= NP_001372133.1:p.Met996=
NM_001385205.1:c.2688G= NP_001372134.1:p.Met896=
NM_001385206.1:c.2652G= NP_001372135.1:p.Met884=
NM_001385207.1:c.2760G= NP_001372136.1:p.Met920=