Canonical Allele Identifier: CA2322387162
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10352453G= , CM000681.2:g.10352453G= GRCh38
NC_000019.9:g.10463129G= , CM000681.1:g.10463129G= GRCh37
NC_000019.8:g.10324129G= NCBI36
NG_007872.1:g.33120C= , LRG_121:g.33120C=

Transcript Alleles

HGVS Amino-acid change
ENST00000524470.2:c.*1648C= ENSP00000514307.1:n.*1648C=
ENST00000525976.6:c.3299C= ENSP00000434831.2:p.Ser1100=
ENST00000527481.3:c.*69C= ENSP00000466340.2:n.*69C=
ENST00000529370.6:n.4675C=
ENST00000529739.2:n.4108C=
ENST00000530829.2:c.*2850C= ENSP00000436826.2:n.*2850C=
ENST00000531836.6:c.3299C= ENSP00000436175.2:p.Ser1100=
ENST00000533334.2:c.*1242+473C= ENSP00000432320.2:n.*1242+473C=
ENST00000534228.2:n.5054+473C=
ENST00000699354.1:n.1401C=
ENST00000699355.1:c.*2799C= ENSP00000514328.1:n.*2799C=
ENST00000699356.1:n.4108C=
ENST00000699357.1:n.5153C=
ENST00000699358.1:c.3200+473C= ENSP00000514329.1:n.3200+473C=
ENST00000699359.1:c.473C=
ENST00000699360.1:c.3257C= ENSP00000514331.1:p.Ser1086=
ENST00000699361.1:n.333C=
ENST00000699362.1:c.195C= ENSP00000514332.1:n.195C=
ENST00000699363.1:c.195C= ENSP00000514333.1:n.195C=
ENST00000699364.1:n.299C=
ENST00000699365.1:c.368C= ENSP00000514334.1:p.Ser123=
ENST00000699366.1:n.111+1361C=
ENST00000699367.1:n.112-1291C=
ENST00000699368.1:c.786C= ENSP00000514335.1:n.786C=
ENST00000525621.6:c.3299C= MANE Select ENSP00000431885.1:p.Ser1100=
ENST00000264818.10:c.3299C= ENSP00000264818.6:p.Ser1100=
ENST00000524462.5:c.2744C= ENSP00000433203.1:p.Ser915=
ENST00000525621.5:c.3299C= ENSP00000431885.1:p.Ser1100=
ENST00000525976.5:c.40C=
ENST00000527481.2:c.476C=
ENST00000529422.1:n.116+569C=
ENST00000529739.1:c.368C= ENSP00000436155.1:p.Ser123=
ENST00000530220.1:n.331+473C=
ENST00000530560.5:c.338-1485C= ENSP00000465291.1:n.338-1485C=
ENST00000592137.1:n.453C=
NM_003331.4:c.3299C= , LRG_121t1:c.3299C= NP_003322.3:p.Ser1100=
XM_011528245.1:c.3299C= XP_011526547.1:p.Ser1100=
XM_011528246.1:c.3002C= XP_011526548.1:p.Ser1001=
XM_011528247.1:c.3002C= XP_011526549.1:p.Ser1001=
XM_011528248.1:c.3200+473C= XP_011526550.1:n.3200+473C=
XM_011528249.1:c.1973C= XP_011526551.1:p.Ser658=
XM_011528251.1:c.1556C= XP_011526553.1:p.Ser519=
XM_011528246.3:c.3002C= XP_011526548.1:p.Ser1001=
XM_011528249.2:c.1973C= XP_011526551.1:p.Ser658=
XR_001753750.1:n.3357+473C=
XR_001753751.1:n.3851C=
XR_002958353.1:n.4777C=
NM_003331.5:c.3299C= MANE Select NP_003322.3:p.Ser1100=
NM_001385197.1:c.3299C= NP_001372126.1:p.Ser1100=
NM_001385198.1:c.3168+505C= NP_001372127.1:n.3168+505C=
NM_001385199.1:c.3113C= NP_001372128.1:p.Ser1038=
NM_001385200.1:c.3296C= NP_001372129.1:p.Ser1099=
NM_001385201.1:c.3101C= NP_001372130.1:p.Ser1034=
NM_001385202.1:c.3215C= NP_001372131.1:p.Ser1072=
NM_001385203.1:c.3380C= NP_001372132.1:p.Ser1127=
NM_001385204.1:c.3509C= NP_001372133.1:p.Ser1170=
NM_001385205.1:c.3209C= NP_001372134.1:p.Ser1070=
NM_001385206.1:c.3173C= NP_001372135.1:p.Ser1058=
NM_001385207.1:c.3281C= NP_001372136.1:p.Ser1094=