Canonical Allele Identifier: CA2322387975
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354048C= , CM000681.2:g.10354048C= GRCh38
NC_000019.9:g.10464724C= , CM000681.1:g.10464724C= GRCh37
NC_000019.8:g.10325724C= NCBI36
NG_007872.1:g.31525G= , LRG_121:g.31525G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1251G= ENSP00000514307.1:n.*1251G=
ENST00000525976.6:c.2902G= ENSP00000434831.2:p.Asp968=
ENST00000527481.3:c.2902G= ENSP00000466340.2:p.Asp968=
ENST00000529370.6:n.4278G=
ENST00000529739.2:n.3316G=
ENST00000530829.2:c.*2453G= ENSP00000436826.2:n.*2453G=
ENST00000531836.6:c.2902G= ENSP00000436175.2:p.Asp968=
ENST00000533334.2:c.*944G= ENSP00000432320.2:n.*944G=
ENST00000534228.2:n.4361G=
ENST00000699354.1:n.1004G=
ENST00000699355.1:c.*2007G= ENSP00000514328.1:n.*2007G=
ENST00000699356.1:n.3316G=
ENST00000699357.1:n.4361G=
ENST00000699358.1:c.2902G= ENSP00000514329.1:p.Asp968=
ENST00000699359.1:c.108G=
ENST00000699360.1:c.2902G= ENSP00000514331.1:p.Asp968=
ENST00000699368.1:c.106G= ENSP00000514335.1:p.Asp36=
ENST00000525621.6:c.2902G= MANE Select ENSP00000431885.1:p.Asp968=
ENST00000264818.10:c.2902G= ENSP00000264818.6:p.Asp968=
ENST00000524462.5:c.2347G= ENSP00000433203.1:p.Asp783=
ENST00000525621.5:c.2902G= ENSP00000431885.1:p.Asp968=
ENST00000527481.2:c.198G=
ENST00000529412.1:n.574G=
ENST00000529739.1:c.-425G= ENSP00000436155.1:n.-425G=
ENST00000530560.5:c.331G= ENSP00000465291.1:p.Asp111=
ENST00000592137.1:n.56G=
NM_003331.4:c.2902G= , LRG_121t1:c.2902G= NP_003322.3:p.Asp968=
XM_011528245.1:c.2902G= XP_011526547.1:p.Asp968=
XM_011528246.1:c.2605G= XP_011526548.1:p.Asp869=
XM_011528247.1:c.2605G= XP_011526549.1:p.Asp869=
XM_011528248.1:c.2902G= XP_011526550.1:p.Asp968=
XM_011528249.1:c.1576G= XP_011526551.1:p.Asp526=
XM_011528251.1:c.1159G= XP_011526553.1:p.Asp387=
XM_011528246.3:c.2605G= XP_011526548.1:p.Asp869=
XM_011528249.2:c.1576G= XP_011526551.1:p.Asp526=
XR_001753750.1:n.3059G=
XR_001753751.1:n.3059G=
XR_002958353.1:n.3985G=
NM_003331.5:c.2902G= MANE Select NP_003322.3:p.Asp968=
NM_001385197.1:c.2902G= NP_001372126.1:p.Asp968=
NM_001385198.1:c.2902G= NP_001372127.1:p.Asp968=
NM_001385199.1:c.2716G= NP_001372128.1:p.Asp906=
NM_001385200.1:c.2899G= NP_001372129.1:p.Asp967=
NM_001385201.1:c.2704G= NP_001372130.1:p.Asp902=
NM_001385202.1:c.2818G= NP_001372131.1:p.Asp940=
NM_001385203.1:c.2983G= NP_001372132.1:p.Asp995=
NM_001385204.1:c.3112G= NP_001372133.1:p.Asp1038=
NM_001385205.1:c.2812G= NP_001372134.1:p.Asp938=
NM_001385206.1:c.2776G= NP_001372135.1:p.Asp926=
NM_001385207.1:c.2884G= NP_001372136.1:p.Asp962=