Canonical Allele Identifier: CA2246160379

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121818C= , CM000679.2:g.8121818C=	GRCh38
NC_000017.10:g.8025136C= , CM000679.1:g.8025136C=	GRCh37
NC_000017.9:g.7965861C=	NCBI36
NG_015807.1:g.2099G=
NG_015816.1:g.7275G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.446G= MANE Select	ENSP00000446205.2:p.Arg149=
ENST00000317814.8:c.431G=	ENSP00000314774.4:p.Arg144=
ENST00000541682.6:c.446G=	ENSP00000446205.2:p.Arg149=
ENST00000577735.1:c.422G=	ENSP00000462491.1:p.Arg141=
NM_001165967.1:c.446G=	NP_001159439.1:p.Arg149=
NM_032580.3:c.431G=	NP_115969.2:p.Arg144=
XM_011524038.1:c.551G=	XP_011522340.1:p.Arg184=
XM_011524039.1:c.542G=	XP_011522341.1:p.Arg181=
XM_011524040.1:c.542G=	XP_011522342.1:p.Arg181=
XM_011524041.1:c.533G=	XP_011522343.1:p.Arg178=
XM_011524042.1:c.404G=	XP_011522344.1:p.Arg135=
XR_934203.1:n.69+2004C=
XM_017025232.1:c.551G=	XP_016880721.1:p.Arg184=
XM_024451007.1:c.551G=	XP_024306775.1:p.Arg184=
NM_001165967.2:c.446G= MANE Select	NP_001159439.1:p.Arg149=
NM_032580.4:c.431G=	NP_115969.2:p.Arg144=