Canonical Allele Identifier: CA2322390534

Gene: TYK2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10359299A= , CM000681.2:g.10359299A=	GRCh38
NC_000019.9:g.10469975A= , CM000681.1:g.10469975A=	GRCh37
NC_000019.8:g.10330975A=	NCBI36
NG_007872.1:g.26274T= , LRG_121:g.26274T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003331.5:c.2051T= MANE Select	NP_003322.3:p.Ile684=
ENST00000525621.6:c.2051T= MANE Select	ENSP00000431885.1:p.Ile684=
NM_001385197.1:c.2051T=	NP_001372126.1:p.Ile684=
NM_001385198.1:c.2051T=	NP_001372127.1:p.Ile684=
NM_001385199.1:c.1865T=	NP_001372128.1:p.Ile622=
NM_001385200.1:c.2051T=	NP_001372129.1:p.Ile684=
NM_001385201.1:c.1853T=	NP_001372130.1:p.Ile618=
NM_001385202.1:c.1967T=	NP_001372131.1:p.Ile656=
NM_001385203.1:c.2051T=	NP_001372132.1:p.Ile684=
NM_001385204.1:c.2051T=	NP_001372133.1:p.Ile684=
NM_001385205.1:c.1961T=	NP_001372134.1:p.Ile654=
NM_001385206.1:c.1925T=	NP_001372135.1:p.Ile642=
NM_001385207.1:c.2033T=	NP_001372136.1:p.Ile678=
NM_003331.4:c.2051T= , LRG_121t1:c.2051T=	NP_003322.3:p.Ile684=
ENST00000264818.10:c.2051T=	ENSP00000264818.6:p.Ile684=
ENST00000524462.5:c.1496T=	ENSP00000433203.1:p.Ile499=
ENST00000524470.2:c.*400T=	ENSP00000514307.1:n.*400T=
ENST00000525621.5:c.2051T=	ENSP00000431885.1:p.Ile684=
ENST00000525976.6:c.2051T=	ENSP00000434831.2:p.Ile684=
ENST00000527481.3:c.2051T=	ENSP00000466340.2:p.Ile684=
ENST00000529370.5:c.2051T=	ENSP00000432728.1:p.Ile684=
ENST00000529370.6:n.2382T=
ENST00000529739.2:n.2465T=
ENST00000530829.2:c.*1602T=	ENSP00000436826.2:n.*1602T=
ENST00000531836.6:c.2051T=	ENSP00000436175.2:p.Ile684=
ENST00000533334.1:c.340T=
ENST00000533334.2:c.*93T=	ENSP00000432320.2:n.*93T=
ENST00000534228.2:n.2465T=
ENST00000699355.1:c.*111T=	ENSP00000514328.1:n.*111T=
ENST00000699356.1:n.2465T=
ENST00000699357.1:n.2465T=
ENST00000699358.1:c.2051T=	ENSP00000514329.1:p.Ile684=
ENST00000699360.1:c.2051T=	ENSP00000514331.1:p.Ile684=
XM_011528245.1:c.2051T=	XP_011526547.1:p.Ile684=
XM_011528246.1:c.1754T=	XP_011526548.1:p.Ile585=
XM_011528246.3:c.1754T=	XP_011526548.1:p.Ile585=
XM_011528247.1:c.1754T=	XP_011526549.1:p.Ile585=
XM_011528248.1:c.2051T=	XP_011526550.1:p.Ile684=
XM_011528249.1:c.725T=	XP_011526551.1:p.Ile242=
XM_011528249.2:c.725T=	XP_011526551.1:p.Ile242=
XM_011528251.1:c.308T=	XP_011526553.1:p.Ile103=
XR_001753750.1:n.2208T=
XR_001753751.1:n.2208T=
XR_001753752.1:n.2320T=
XR_002958353.1:n.2089T=