Canonical Allele Identifier: CA2322387976
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354050T= , CM000681.2:g.10354050T= GRCh38
NC_000019.9:g.10464726T= , CM000681.1:g.10464726T= GRCh37
NC_000019.8:g.10325726T= NCBI36
NG_007872.1:g.31523A= , LRG_121:g.31523A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1249A= ENSP00000514307.1:n.*1249A=
ENST00000525976.6:c.2900A= ENSP00000434831.2:p.Glu967=
ENST00000527481.3:c.2900A= ENSP00000466340.2:p.Glu967=
ENST00000529370.6:n.4276A=
ENST00000529739.2:n.3314A=
ENST00000530829.2:c.*2451A= ENSP00000436826.2:n.*2451A=
ENST00000531836.6:c.2900A= ENSP00000436175.2:p.Glu967=
ENST00000533334.2:c.*942A= ENSP00000432320.2:n.*942A=
ENST00000534228.2:n.4359A=
ENST00000699354.1:n.1002A=
ENST00000699355.1:c.*2005A= ENSP00000514328.1:n.*2005A=
ENST00000699356.1:n.3314A=
ENST00000699357.1:n.4359A=
ENST00000699358.1:c.2900A= ENSP00000514329.1:p.Glu967=
ENST00000699359.1:c.106A=
ENST00000699360.1:c.2900A= ENSP00000514331.1:p.Glu967=
ENST00000699368.1:c.104A= ENSP00000514335.1:p.Glu35=
ENST00000525621.6:c.2900A= MANE Select ENSP00000431885.1:p.Glu967=
ENST00000264818.10:c.2900A= ENSP00000264818.6:p.Glu967=
ENST00000524462.5:c.2345A= ENSP00000433203.1:p.Glu782=
ENST00000525621.5:c.2900A= ENSP00000431885.1:p.Glu967=
ENST00000527481.2:c.196A=
ENST00000529412.1:n.572A=
ENST00000529739.1:c.-427A= ENSP00000436155.1:n.-427A=
ENST00000530560.5:c.329A= ENSP00000465291.1:p.Glu110=
ENST00000592137.1:n.54A=
NM_003331.4:c.2900A= , LRG_121t1:c.2900A= NP_003322.3:p.Glu967=
XM_011528245.1:c.2900A= XP_011526547.1:p.Glu967=
XM_011528246.1:c.2603A= XP_011526548.1:p.Glu868=
XM_011528247.1:c.2603A= XP_011526549.1:p.Glu868=
XM_011528248.1:c.2900A= XP_011526550.1:p.Glu967=
XM_011528249.1:c.1574A= XP_011526551.1:p.Glu525=
XM_011528251.1:c.1157A= XP_011526553.1:p.Glu386=
XM_011528246.3:c.2603A= XP_011526548.1:p.Glu868=
XM_011528249.2:c.1574A= XP_011526551.1:p.Glu525=
XR_001753750.1:n.3057A=
XR_001753751.1:n.3057A=
XR_002958353.1:n.3983A=
NM_003331.5:c.2900A= MANE Select NP_003322.3:p.Glu967=
NM_001385197.1:c.2900A= NP_001372126.1:p.Glu967=
NM_001385198.1:c.2900A= NP_001372127.1:p.Glu967=
NM_001385199.1:c.2714A= NP_001372128.1:p.Glu905=
NM_001385200.1:c.2897A= NP_001372129.1:p.Glu966=
NM_001385201.1:c.2702A= NP_001372130.1:p.Glu901=
NM_001385202.1:c.2816A= NP_001372131.1:p.Glu939=
NM_001385203.1:c.2981A= NP_001372132.1:p.Glu994=
NM_001385204.1:c.3110A= NP_001372133.1:p.Glu1037=
NM_001385205.1:c.2810A= NP_001372134.1:p.Glu937=
NM_001385206.1:c.2774A= NP_001372135.1:p.Glu925=
NM_001385207.1:c.2882A= NP_001372136.1:p.Glu961=