Canonical Allele Identifier: CA2322388048
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354195T= , CM000681.2:g.10354195T= GRCh38
NC_000019.9:g.10464871T= , CM000681.1:g.10464871T= GRCh37
NC_000019.8:g.10325871T= NCBI36
NG_007872.1:g.31378A= , LRG_121:g.31378A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1104A= ENSP00000514307.1:n.*1104A=
ENST00000525976.6:c.2755A= ENSP00000434831.2:p.Thr919=
ENST00000527481.3:c.2755A= ENSP00000466340.2:p.Thr919=
ENST00000529370.6:n.4131A=
ENST00000529739.2:n.3169A=
ENST00000530829.2:c.*2306A= ENSP00000436826.2:n.*2306A=
ENST00000531836.6:c.2755A= ENSP00000436175.2:p.Thr919=
ENST00000533334.2:c.*797A= ENSP00000432320.2:n.*797A=
ENST00000534228.2:n.4214A=
ENST00000699354.1:n.857A=
ENST00000699355.1:c.*1860A= ENSP00000514328.1:n.*1860A=
ENST00000699356.1:n.3169A=
ENST00000699357.1:n.4214A=
ENST00000699358.1:c.2755A= ENSP00000514329.1:p.Thr919=
ENST00000699360.1:c.2755A= ENSP00000514331.1:p.Thr919=
ENST00000525621.6:c.2755A= MANE Select ENSP00000431885.1:p.Thr919=
ENST00000264818.10:c.2755A= ENSP00000264818.6:p.Thr919=
ENST00000524462.5:c.2200A= ENSP00000433203.1:p.Thr734=
ENST00000525621.5:c.2755A= ENSP00000431885.1:p.Thr919=
ENST00000527481.2:c.51A=
ENST00000529412.1:n.427A=
ENST00000530560.5:c.184A= ENSP00000465291.1:p.Thr62=
NM_003331.4:c.2755A= , LRG_121t1:c.2755A= NP_003322.3:p.Thr919=
XM_011528245.1:c.2755A= XP_011526547.1:p.Thr919=
XM_011528246.1:c.2458A= XP_011526548.1:p.Thr820=
XM_011528247.1:c.2458A= XP_011526549.1:p.Thr820=
XM_011528248.1:c.2755A= XP_011526550.1:p.Thr919=
XM_011528249.1:c.1429A= XP_011526551.1:p.Thr477=
XM_011528251.1:c.1012A= XP_011526553.1:p.Thr338=
XM_011528246.3:c.2458A= XP_011526548.1:p.Thr820=
XM_011528249.2:c.1429A= XP_011526551.1:p.Thr477=
XR_001753750.1:n.2912A=
XR_001753751.1:n.2912A=
XR_002958353.1:n.3838A=
NM_003331.5:c.2755A= MANE Select NP_003322.3:p.Thr919=
NM_001385197.1:c.2755A= NP_001372126.1:p.Thr919=
NM_001385198.1:c.2755A= NP_001372127.1:p.Thr919=
NM_001385199.1:c.2569A= NP_001372128.1:p.Thr857=
NM_001385200.1:c.2752A= NP_001372129.1:p.Thr918=
NM_001385201.1:c.2557A= NP_001372130.1:p.Thr853=
NM_001385202.1:c.2671A= NP_001372131.1:p.Thr891=
NM_001385203.1:c.2836A= NP_001372132.1:p.Thr946=
NM_001385204.1:c.2965A= NP_001372133.1:p.Thr989=
NM_001385205.1:c.2665A= NP_001372134.1:p.Thr889=
NM_001385206.1:c.2629A= NP_001372135.1:p.Thr877=
NM_001385207.1:c.2737A= NP_001372136.1:p.Thr913=