Canonical Allele Identifier: CA2322389808
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10357879A= , CM000681.2:g.10357879A= GRCh38
NC_000019.9:g.10468555A= , CM000681.1:g.10468555A= GRCh37
NC_000019.8:g.10329555A= NCBI36
NG_007872.1:g.27694T= , LRG_121:g.27694T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*700T= ENSP00000514307.1:n.*700T=
ENST00000525976.6:c.2351T= ENSP00000434831.2:p.Leu784=
ENST00000527481.3:c.2351T= ENSP00000466340.2:p.Leu784=
ENST00000529370.6:n.2682T=
ENST00000529739.2:n.2765T=
ENST00000530829.2:c.*1902T= ENSP00000436826.2:n.*1902T=
ENST00000531836.6:c.2351T= ENSP00000436175.2:p.Leu784=
ENST00000533334.2:c.*393T= ENSP00000432320.2:n.*393T=
ENST00000534228.2:n.2765T=
ENST00000699354.1:n.453T=
ENST00000699355.1:c.*411T= ENSP00000514328.1:n.*411T=
ENST00000699356.1:n.2765T=
ENST00000699357.1:n.2765T=
ENST00000699358.1:c.2351T= ENSP00000514329.1:p.Leu784=
ENST00000699360.1:c.2351T= ENSP00000514331.1:p.Leu784=
ENST00000525621.6:c.2351T= MANE Select ENSP00000431885.1:p.Leu784=
ENST00000264818.10:c.2351T= ENSP00000264818.6:p.Leu784=
ENST00000524462.5:c.1796T= ENSP00000433203.1:p.Leu599=
ENST00000525621.5:c.2351T= ENSP00000431885.1:p.Leu784=
ENST00000529370.5:c.2351T= ENSP00000432728.1:p.Leu784=
ENST00000529412.1:n.23T=
ENST00000533334.1:c.640T=
NM_003331.4:c.2351T= , LRG_121t1:c.2351T= NP_003322.3:p.Leu784=
XM_011528245.1:c.2351T= XP_011526547.1:p.Leu784=
XM_011528246.1:c.2054T= XP_011526548.1:p.Leu685=
XM_011528247.1:c.2054T= XP_011526549.1:p.Leu685=
XM_011528248.1:c.2351T= XP_011526550.1:p.Leu784=
XM_011528249.1:c.1025T= XP_011526551.1:p.Leu342=
XM_011528251.1:c.608T= XP_011526553.1:p.Leu203=
XM_011528246.3:c.2054T= XP_011526548.1:p.Leu685=
XM_011528249.2:c.1025T= XP_011526551.1:p.Leu342=
XR_001753750.1:n.2508T=
XR_001753751.1:n.2508T=
XR_001753752.1:n.2620T=
XR_002958353.1:n.2389T=
NM_003331.5:c.2351T= MANE Select NP_003322.3:p.Leu784=
NM_001385197.1:c.2351T= NP_001372126.1:p.Leu784=
NM_001385198.1:c.2351T= NP_001372127.1:p.Leu784=
NM_001385199.1:c.2165T= NP_001372128.1:p.Leu722=
NM_001385200.1:c.2351T= NP_001372129.1:p.Leu784=
NM_001385201.1:c.2153T= NP_001372130.1:p.Leu718=
NM_001385202.1:c.2267T= NP_001372131.1:p.Leu756=
NM_001385203.1:c.2351T= NP_001372132.1:p.Leu784=
NM_001385204.1:c.2351T= NP_001372133.1:p.Leu784=
NM_001385205.1:c.2261T= NP_001372134.1:p.Leu754=
NM_001385206.1:c.2225T= NP_001372135.1:p.Leu742=
NM_001385207.1:c.2333T= NP_001372136.1:p.Leu778=