Canonical Allele Identifier: CA2322387368
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10352644C= , CM000681.2:g.10352644C= GRCh38
NC_000019.9:g.10463320C= , CM000681.1:g.10463320C= GRCh37
NC_000019.8:g.10324320C= NCBI36
NG_007872.1:g.32929G= , LRG_121:g.32929G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1550-93G= ENSP00000514307.1:n.*1550-93G=
ENST00000525976.6:c.3201-93G= ENSP00000434831.2:n.3201-93G=
ENST00000527481.3:c.3082-93G= ENSP00000466340.2:n.3082-93G=
ENST00000529370.6:n.4577-93G=
ENST00000529739.2:n.4010-93G=
ENST00000530829.2:c.*2752-93G= ENSP00000436826.2:n.*2752-93G=
ENST00000531836.6:c.3201-93G= ENSP00000436175.2:n.3201-93G=
ENST00000533334.2:c.*1242+282G= ENSP00000432320.2:n.*1242+282G=
ENST00000534228.2:n.5054+282G=
ENST00000699354.1:n.1303-93G=
ENST00000699355.1:c.*2701-93G= ENSP00000514328.1:n.*2701-93G=
ENST00000699356.1:n.4010-93G=
ENST00000699357.1:n.5055-93G=
ENST00000699358.1:c.3200+282G= ENSP00000514329.1:n.3200+282G=
ENST00000699359.1:c.375-93G=
ENST00000699360.1:c.3159-93G= ENSP00000514331.1:n.3159-93G=
ENST00000699361.1:n.142G=
ENST00000699362.1:c.97-93G= ENSP00000514332.1:n.97-93G=
ENST00000699363.1:c.97-93G= ENSP00000514333.1:n.97-93G=
ENST00000699364.1:n.201-93G=
ENST00000699365.1:c.270-93G= ENSP00000514334.1:n.270-93G=
ENST00000699366.1:n.111+1170G=
ENST00000699367.1:n.111+1170G=
ENST00000699368.1:c.688-93G= ENSP00000514335.1:n.688-93G=
ENST00000525621.6:c.3201-93G= MANE Select ENSP00000431885.1:n.3201-93G=
ENST00000264818.10:c.3201-93G= ENSP00000264818.6:n.3201-93G=
ENST00000524462.5:c.2646-93G= ENSP00000433203.1:n.2646-93G=
ENST00000525621.5:c.3201-93G= ENSP00000431885.1:n.3201-93G=
ENST00000527481.2:c.378-93G=
ENST00000529422.1:n.116+378G=
ENST00000529739.1:c.270-93G= ENSP00000436155.1:n.270-93G=
ENST00000530220.1:n.331+282G=
ENST00000530560.5:c.337+1398G= ENSP00000465291.1:n.337+1398G=
ENST00000592137.1:n.355-93G=
NM_003331.4:c.3201-93G= , LRG_121t1:c.3201-93G= NP_003322.3:n.3201-93G=
XM_011528245.1:c.3201-93G= XP_011526547.1:n.3201-93G=
XM_011528246.1:c.2904-93G= XP_011526548.1:n.2904-93G=
XM_011528247.1:c.2904-93G= XP_011526549.1:n.2904-93G=
XM_011528248.1:c.3200+282G= XP_011526550.1:n.3200+282G=
XM_011528249.1:c.1875-93G= XP_011526551.1:n.1875-93G=
XM_011528251.1:c.1458-93G= XP_011526553.1:n.1458-93G=
XM_011528246.3:c.2904-93G= XP_011526548.1:n.2904-93G=
XM_011528249.2:c.1875-93G= XP_011526551.1:n.1875-93G=
XR_001753750.1:n.3357+282G=
XR_001753751.1:n.3753-93G=
XR_002958353.1:n.4679-93G=
NM_003331.5:c.3201-93G= MANE Select NP_003322.3:n.3201-93G=
NM_001385197.1:c.3201-93G= NP_001372126.1:n.3201-93G=
NM_001385198.1:c.3168+314G= NP_001372127.1:n.3168+314G=
NM_001385199.1:c.3015-93G= NP_001372128.1:n.3015-93G=
NM_001385200.1:c.3198-93G= NP_001372129.1:n.3198-93G=
NM_001385201.1:c.3003-93G= NP_001372130.1:n.3003-93G=
NM_001385202.1:c.3117-93G= NP_001372131.1:n.3117-93G=
NM_001385203.1:c.3282-93G= NP_001372132.1:n.3282-93G=
NM_001385204.1:c.3411-93G= NP_001372133.1:n.3411-93G=
NM_001385205.1:c.3111-93G= NP_001372134.1:n.3111-93G=
NM_001385206.1:c.3075-93G= NP_001372135.1:n.3075-93G=
NM_001385207.1:c.3183-93G= NP_001372136.1:n.3183-93G=