Canonical Allele Identifier: CA2322389776
Gene: TYK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10357803A= , CM000681.2:g.10357803A= GRCh38
NC_000019.9:g.10468479A= , CM000681.1:g.10468479A= GRCh37
NC_000019.8:g.10329479A= NCBI36
NG_007872.1:g.27770T= , LRG_121:g.27770T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000524470.2:c.*776T= ENSP00000514307.1:n.*776T=
ENST00000525976.6:c.2427T= ENSP00000434831.2:p.Phe809=
ENST00000527481.3:c.2427T= ENSP00000466340.2:p.Phe809=
ENST00000529370.6:n.2758T=
ENST00000529739.2:n.2841T=
ENST00000530829.2:c.*1978T= ENSP00000436826.2:n.*1978T=
ENST00000531836.6:c.2427T= ENSP00000436175.2:p.Phe809=
ENST00000533334.2:c.*469T= ENSP00000432320.2:n.*469T=
ENST00000534228.2:n.2841T=
ENST00000699354.1:n.529T=
ENST00000699355.1:c.*487T= ENSP00000514328.1:n.*487T=
ENST00000699356.1:n.2841T=
ENST00000699357.1:n.2841T=
ENST00000699358.1:c.2427T= ENSP00000514329.1:p.Phe809=
ENST00000699360.1:c.2427T= ENSP00000514331.1:p.Phe809=
ENST00000525621.6:c.2427T= MANE Select ENSP00000431885.1:p.Phe809=
ENST00000264818.10:c.2427T= ENSP00000264818.6:p.Phe809=
ENST00000524462.5:c.1872T= ENSP00000433203.1:p.Phe624=
ENST00000525621.5:c.2427T= ENSP00000431885.1:p.Phe809=
ENST00000529370.5:c.2427T= ENSP00000432728.1:p.Phe809=
ENST00000529412.1:n.99T=
ENST00000533334.1:c.716T=
NM_003331.4:c.2427T= , LRG_121t1:c.2427T= NP_003322.3:p.Phe809=
XM_011528245.1:c.2427T= XP_011526547.1:p.Phe809=
XM_011528246.1:c.2130T= XP_011526548.1:p.Phe710=
XM_011528247.1:c.2130T= XP_011526549.1:p.Phe710=
XM_011528248.1:c.2427T= XP_011526550.1:p.Phe809=
XM_011528249.1:c.1101T= XP_011526551.1:p.Phe367=
XM_011528251.1:c.684T= XP_011526553.1:p.Phe228=
XM_011528246.3:c.2130T= XP_011526548.1:p.Phe710=
XM_011528249.2:c.1101T= XP_011526551.1:p.Phe367=
XR_001753750.1:n.2584T=
XR_001753751.1:n.2584T=
XR_002958353.1:n.2465T=
NM_003331.5:c.2427T= MANE Select NP_003322.3:p.Phe809=
NM_001385197.1:c.2427T= NP_001372126.1:p.Phe809=
NM_001385198.1:c.2427T= NP_001372127.1:p.Phe809=
NM_001385199.1:c.2241T= NP_001372128.1:p.Phe747=
NM_001385200.1:c.2427T= NP_001372129.1:p.Phe809=
NM_001385201.1:c.2229T= NP_001372130.1:p.Phe743=
NM_001385202.1:c.2343T= NP_001372131.1:p.Phe781=
NM_001385203.1:c.2427T= NP_001372132.1:p.Phe809=
NM_001385204.1:c.2427T= NP_001372133.1:p.Phe809=
NM_001385205.1:c.2337T= NP_001372134.1:p.Phe779=
NM_001385206.1:c.2301T= NP_001372135.1:p.Phe767=
NM_001385207.1:c.2409T= NP_001372136.1:p.Phe803=