Canonical Allele Identifier: CA2322387151
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10352443G= , CM000681.2:g.10352443G= GRCh38
NC_000019.9:g.10463119G= , CM000681.1:g.10463119G= GRCh37
NC_000019.8:g.10324119G= NCBI36
NG_007872.1:g.33130C= , LRG_121:g.33130C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524470.2:c.*1658C= ENSP00000514307.1:n.*1658C=
ENST00000525976.6:c.3309C= ENSP00000434831.2:p.Ser1103=
ENST00000527481.3:c.*79C= ENSP00000466340.2:n.*79C=
ENST00000529370.6:n.4685C=
ENST00000529739.2:n.4118C=
ENST00000530829.2:c.*2860C= ENSP00000436826.2:n.*2860C=
ENST00000531836.6:c.3309C= ENSP00000436175.2:p.Ser1103=
ENST00000533334.2:c.*1242+483C= ENSP00000432320.2:n.*1242+483C=
ENST00000534228.2:n.5054+483C=
ENST00000699354.1:n.1411C=
ENST00000699355.1:c.*2809C= ENSP00000514328.1:n.*2809C=
ENST00000699356.1:n.4118C=
ENST00000699357.1:n.5163C=
ENST00000699358.1:c.3200+483C= ENSP00000514329.1:n.3200+483C=
ENST00000699359.1:c.483C=
ENST00000699360.1:c.3267C= ENSP00000514331.1:p.Ser1089=
ENST00000699361.1:n.343C=
ENST00000699362.1:c.205C= ENSP00000514332.1:n.205C=
ENST00000699363.1:c.205C= ENSP00000514333.1:n.205C=
ENST00000699364.1:n.309C=
ENST00000699365.1:c.378C= ENSP00000514334.1:p.Ser126=
ENST00000699366.1:n.111+1371C=
ENST00000699367.1:n.112-1281C=
ENST00000699368.1:c.796C= ENSP00000514335.1:n.796C=
ENST00000525621.6:c.3309C= MANE Select ENSP00000431885.1:p.Ser1103=
ENST00000264818.10:c.3309C= ENSP00000264818.6:p.Ser1103=
ENST00000524462.5:c.2754C= ENSP00000433203.1:p.Ser918=
ENST00000525621.5:c.3309C= ENSP00000431885.1:p.Ser1103=
ENST00000525976.5:c.50C=
ENST00000527481.2:c.486C=
ENST00000529422.1:n.116+579C=
ENST00000529739.1:c.378C= ENSP00000436155.1:p.Ser126=
ENST00000530220.1:n.331+483C=
ENST00000530560.5:c.338-1475C= ENSP00000465291.1:n.338-1475C=
ENST00000592137.1:n.463C=
NM_003331.4:c.3309C= , LRG_121t1:c.3309C= NP_003322.3:p.Ser1103=
XM_011528245.1:c.3309C= XP_011526547.1:p.Ser1103=
XM_011528246.1:c.3012C= XP_011526548.1:p.Ser1004=
XM_011528247.1:c.3012C= XP_011526549.1:p.Ser1004=
XM_011528248.1:c.3200+483C= XP_011526550.1:n.3200+483C=
XM_011528249.1:c.1983C= XP_011526551.1:p.Ser661=
XM_011528251.1:c.1566C= XP_011526553.1:p.Ser522=
XM_011528246.3:c.3012C= XP_011526548.1:p.Ser1004=
XM_011528249.2:c.1983C= XP_011526551.1:p.Ser661=
XR_001753750.1:n.3357+483C=
XR_001753751.1:n.3861C=
XR_002958353.1:n.4787C=
NM_003331.5:c.3309C= MANE Select NP_003322.3:p.Ser1103=
NM_001385197.1:c.3309C= NP_001372126.1:p.Ser1103=
NM_001385198.1:c.3168+515C= NP_001372127.1:n.3168+515C=
NM_001385199.1:c.3123C= NP_001372128.1:p.Ser1041=
NM_001385200.1:c.3306C= NP_001372129.1:p.Ser1102=
NM_001385201.1:c.3111C= NP_001372130.1:p.Ser1037=
NM_001385202.1:c.3225C= NP_001372131.1:p.Ser1075=
NM_001385203.1:c.3390C= NP_001372132.1:p.Ser1130=
NM_001385204.1:c.3519C= NP_001372133.1:p.Ser1173=
NM_001385205.1:c.3219C= NP_001372134.1:p.Ser1073=
NM_001385206.1:c.3183C= NP_001372135.1:p.Ser1061=
NM_001385207.1:c.3291C= NP_001372136.1:p.Ser1097=