Canonical Allele Identifier: CA403988784
Gene: TYK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354182G>C , CM000681.2:g.10354182G>C GRCh38
NC_000019.9:g.10464858G>C , CM000681.1:g.10464858G>C GRCh37
NC_000019.8:g.10325858G>C NCBI36
NG_007872.1:g.31391C>G , LRG_121:g.31391C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1117C>G ENSP00000514307.1:n.*1117C>G
ENST00000525976.6:c.2768C>G ENSP00000434831.2:p.Thr923Ser
ENST00000527481.3:c.2768C>G ENSP00000466340.2:p.Thr923Ser
ENST00000529370.6:n.4144C>G
ENST00000529739.2:n.3182C>G
ENST00000530829.2:c.*2319C>G ENSP00000436826.2:n.*2319C>G
ENST00000531836.6:c.2768C>G ENSP00000436175.2:p.Thr923Ser
ENST00000533334.2:c.*810C>G ENSP00000432320.2:n.*810C>G
ENST00000534228.2:n.4227C>G
ENST00000699354.1:n.870C>G
ENST00000699355.1:c.*1873C>G ENSP00000514328.1:n.*1873C>G
ENST00000699356.1:n.3182C>G
ENST00000699357.1:n.4227C>G
ENST00000699358.1:c.2768C>G ENSP00000514329.1:p.Thr923Ser
ENST00000699360.1:c.2768C>G ENSP00000514331.1:p.Thr923Ser
ENST00000525621.6:c.2768C>G MANE Select ENSP00000431885.1:p.Thr923Ser
ENST00000264818.10:c.2768C>G ENSP00000264818.6:p.Thr923Ser
ENST00000524462.5:c.2213C>G ENSP00000433203.1:p.Thr738Ser
ENST00000525621.5:c.2768C>G ENSP00000431885.1:p.Thr923Ser
ENST00000527481.2:c.64C>G
ENST00000529412.1:n.440C>G
ENST00000530560.5:c.197C>G ENSP00000465291.1:p.Thr66Ser
NM_003331.4:c.2768C>G , LRG_121t1:c.2768C>G NP_003322.3:p.Thr923Ser
XM_011528245.1:c.2768C>G XP_011526547.1:p.Thr923Ser
XM_011528246.1:c.2471C>G XP_011526548.1:p.Thr824Ser
XM_011528247.1:c.2471C>G XP_011526549.1:p.Thr824Ser
XM_011528248.1:c.2768C>G XP_011526550.1:p.Thr923Ser
XM_011528249.1:c.1442C>G XP_011526551.1:p.Thr481Ser
XM_011528251.1:c.1025C>G XP_011526553.1:p.Thr342Ser
XM_011528246.3:c.2471C>G XP_011526548.1:p.Thr824Ser
XM_011528249.2:c.1442C>G XP_011526551.1:p.Thr481Ser
XR_001753750.1:n.2925C>G
XR_001753751.1:n.2925C>G
XR_002958353.1:n.3851C>G
NM_003331.5:c.2768C>G MANE Select NP_003322.3:p.Thr923Ser
NM_001385197.1:c.2768C>G NP_001372126.1:p.Thr923Ser
NM_001385198.1:c.2768C>G NP_001372127.1:p.Thr923Ser
NM_001385199.1:c.2582C>G NP_001372128.1:p.Thr861Ser
NM_001385200.1:c.2765C>G NP_001372129.1:p.Thr922Ser
NM_001385201.1:c.2570C>G NP_001372130.1:p.Thr857Ser
NM_001385202.1:c.2684C>G NP_001372131.1:p.Thr895Ser
NM_001385203.1:c.2849C>G NP_001372132.1:p.Thr950Ser
NM_001385204.1:c.2978C>G NP_001372133.1:p.Thr993Ser
NM_001385205.1:c.2678C>G NP_001372134.1:p.Thr893Ser
NM_001385206.1:c.2642C>G NP_001372135.1:p.Thr881Ser
NM_001385207.1:c.2750C>G NP_001372136.1:p.Thr917Ser