Canonical Allele Identifier: CA2322388020
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10354133C= , CM000681.2:g.10354133C= GRCh38
NC_000019.9:g.10464809C= , CM000681.1:g.10464809C= GRCh37
NC_000019.8:g.10325809C= NCBI36
NG_007872.1:g.31440G= , LRG_121:g.31440G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*1166G= ENSP00000514307.1:n.*1166G=
ENST00000525976.6:c.2817G= ENSP00000434831.2:p.Gln939=
ENST00000527481.3:c.2817G= ENSP00000466340.2:p.Gln939=
ENST00000529370.6:n.4193G=
ENST00000529739.2:n.3231G=
ENST00000530829.2:c.*2368G= ENSP00000436826.2:n.*2368G=
ENST00000531836.6:c.2817G= ENSP00000436175.2:p.Gln939=
ENST00000533334.2:c.*859G= ENSP00000432320.2:n.*859G=
ENST00000534228.2:n.4276G=
ENST00000699354.1:n.919G=
ENST00000699355.1:c.*1922G= ENSP00000514328.1:n.*1922G=
ENST00000699356.1:n.3231G=
ENST00000699357.1:n.4276G=
ENST00000699358.1:c.2817G= ENSP00000514329.1:p.Gln939=
ENST00000699359.1:c.23G=
ENST00000699360.1:c.2817G= ENSP00000514331.1:p.Gln939=
ENST00000699368.1:c.21G= ENSP00000514335.1:p.Gln7=
ENST00000525621.6:c.2817G= MANE Select ENSP00000431885.1:p.Gln939=
ENST00000264818.10:c.2817G= ENSP00000264818.6:p.Gln939=
ENST00000524462.5:c.2262G= ENSP00000433203.1:p.Gln754=
ENST00000525621.5:c.2817G= ENSP00000431885.1:p.Gln939=
ENST00000527481.2:c.113G=
ENST00000529412.1:n.489G=
ENST00000530560.5:c.246G= ENSP00000465291.1:p.Gln82=
NM_003331.4:c.2817G= , LRG_121t1:c.2817G= NP_003322.3:p.Gln939=
XM_011528245.1:c.2817G= XP_011526547.1:p.Gln939=
XM_011528246.1:c.2520G= XP_011526548.1:p.Gln840=
XM_011528247.1:c.2520G= XP_011526549.1:p.Gln840=
XM_011528248.1:c.2817G= XP_011526550.1:p.Gln939=
XM_011528249.1:c.1491G= XP_011526551.1:p.Gln497=
XM_011528251.1:c.1074G= XP_011526553.1:p.Gln358=
XM_011528246.3:c.2520G= XP_011526548.1:p.Gln840=
XM_011528249.2:c.1491G= XP_011526551.1:p.Gln497=
XR_001753750.1:n.2974G=
XR_001753751.1:n.2974G=
XR_002958353.1:n.3900G=
NM_003331.5:c.2817G= MANE Select NP_003322.3:p.Gln939=
NM_001385197.1:c.2817G= NP_001372126.1:p.Gln939=
NM_001385198.1:c.2817G= NP_001372127.1:p.Gln939=
NM_001385199.1:c.2631G= NP_001372128.1:p.Gln877=
NM_001385200.1:c.2814G= NP_001372129.1:p.Gln938=
NM_001385201.1:c.2619G= NP_001372130.1:p.Gln873=
NM_001385202.1:c.2733G= NP_001372131.1:p.Gln911=
NM_001385203.1:c.2898G= NP_001372132.1:p.Gln966=
NM_001385204.1:c.3027G= NP_001372133.1:p.Gln1009=
NM_001385205.1:c.2727G= NP_001372134.1:p.Gln909=
NM_001385206.1:c.2691G= NP_001372135.1:p.Gln897=
NM_001385207.1:c.2799G= NP_001372136.1:p.Gln933=