Canonical Allele Identifier: CA631997799
Gene: TYK2 HGNC NCBI

Linked Data

dbSNP Id: rs1270557692

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354057_10354058insTGATGT , CM000681.2:g.10354057_10354058insTGATGT GRCh38
NC_000019.9:g.10464733_10464734insTGATGT , CM000681.1:g.10464733_10464734insTGATGT GRCh37
NC_000019.8:g.10325733_10325734insTGATGT NCBI36
NG_007872.1:g.31515_31516insACATCA , LRG_121:g.31515_31516insACATCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1241_*1242insACATCA ENSP00000514307.1:n.*1241_*1242insACATCA
ENST00000525976.6:c.2892_2893insACATCA ENSP00000434831.2:p.Gly964_Cys965insThrSer
ENST00000527481.3:c.2892_2893insACATCA ENSP00000466340.2:p.Gly964_Cys965insThrSer
ENST00000529370.6:n.4268_4269insACATCA
ENST00000529739.2:n.3306_3307insACATCA
ENST00000530829.2:c.*2443_*2444insACATCA ENSP00000436826.2:n.*2443_*2444insACATCA
ENST00000531836.6:c.2892_2893insACATCA ENSP00000436175.2:p.Gly964_Cys965insThrSer
ENST00000533334.2:c.*934_*935insACATCA ENSP00000432320.2:n.*934_*935insACATCA
ENST00000534228.2:n.4351_4352insACATCA
ENST00000699354.1:n.994_995insACATCA
ENST00000699355.1:c.*1997_*1998insACATCA ENSP00000514328.1:n.*1997_*1998insACATCA
ENST00000699356.1:n.3306_3307insACATCA
ENST00000699357.1:n.4351_4352insACATCA
ENST00000699358.1:c.2892_2893insACATCA ENSP00000514329.1:p.Gly964_Cys965insThrSer
ENST00000699359.1:c.98_99insACATCA
ENST00000699360.1:c.2892_2893insACATCA ENSP00000514331.1:p.Gly964_Cys965insThrSer
ENST00000699368.1:c.96_97insACATCA ENSP00000514335.1:p.Gly32_Cys33insThrSer
ENST00000525621.6:c.2892_2893insACATCA MANE Select ENSP00000431885.1:p.Gly964_Cys965insThrSer
ENST00000264818.10:c.2892_2893insACATCA ENSP00000264818.6:p.Gly964_Cys965insThrSer
ENST00000524462.5:c.2337_2338insACATCA ENSP00000433203.1:p.Gly779_Cys780insThrSer
ENST00000525621.5:c.2892_2893insACATCA ENSP00000431885.1:p.Gly964_Cys965insThrSer
ENST00000527481.2:c.188_189insACATCA
ENST00000529412.1:n.564_565insACATCA
ENST00000529739.1:c.-435_-434insACATCA ENSP00000436155.1:n.-435_-434insACATCA
ENST00000530560.5:c.321_322insACATCA ENSP00000465291.1:p.Gly107_Cys108insThrSer
ENST00000592137.1:n.46_47insACATCA
NM_003331.4:c.2892_2893insACATCA , LRG_121t1:c.2892_2893insACATCA NP_003322.3:p.Gly964_Cys965insThrSer
XM_011528245.1:c.2892_2893insACATCA XP_011526547.1:p.Gly964_Cys965insThrSer
XM_011528246.1:c.2595_2596insACATCA XP_011526548.1:p.Gly865_Cys866insThrSer
XM_011528247.1:c.2595_2596insACATCA XP_011526549.1:p.Gly865_Cys866insThrSer
XM_011528248.1:c.2892_2893insACATCA XP_011526550.1:p.Gly964_Cys965insThrSer
XM_011528249.1:c.1566_1567insACATCA XP_011526551.1:p.Gly522_Cys523insThrSer
XM_011528251.1:c.1149_1150insACATCA XP_011526553.1:p.Gly383_Cys384insThrSer
XM_011528246.3:c.2595_2596insACATCA XP_011526548.1:p.Gly865_Cys866insThrSer
XM_011528249.2:c.1566_1567insACATCA XP_011526551.1:p.Gly522_Cys523insThrSer
XR_001753750.1:n.3049_3050insACATCA
XR_001753751.1:n.3049_3050insACATCA
XR_002958353.1:n.3975_3976insACATCA
NM_003331.5:c.2892_2893insACATCA MANE Select NP_003322.3:p.Gly964_Cys965insThrSer
NM_001385197.1:c.2892_2893insACATCA NP_001372126.1:p.Gly964_Cys965insThrSer
NM_001385198.1:c.2892_2893insACATCA NP_001372127.1:p.Gly964_Cys965insThrSer
NM_001385199.1:c.2706_2707insACATCA NP_001372128.1:p.Gly902_Cys903insThrSer
NM_001385200.1:c.2889_2890insACATCA NP_001372129.1:p.Gly963_Cys964insThrSer
NM_001385201.1:c.2694_2695insACATCA NP_001372130.1:p.Gly898_Cys899insThrSer
NM_001385202.1:c.2808_2809insACATCA NP_001372131.1:p.Gly936_Cys937insThrSer
NM_001385203.1:c.2973_2974insACATCA NP_001372132.1:p.Gly991_Cys992insThrSer
NM_001385204.1:c.3102_3103insACATCA NP_001372133.1:p.Gly1034_Cys1035insThrSer
NM_001385205.1:c.2802_2803insACATCA NP_001372134.1:p.Gly934_Cys935insThrSer
NM_001385206.1:c.2766_2767insACATCA NP_001372135.1:p.Gly922_Cys923insThrSer
NM_001385207.1:c.2874_2875insACATCA NP_001372136.1:p.Gly958_Cys959insThrSer