Canonical Allele Identifier: CA2246160642

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121892G= , CM000679.2:g.8121892G=	GRCh38
NC_000017.10:g.8025210G= , CM000679.1:g.8025210G=	GRCh37
NC_000017.9:g.7965935G=	NCBI36
NG_015807.1:g.2025C=
NG_015816.1:g.7201C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.372C= MANE Select	ENSP00000446205.2:p.Phe124=
ENST00000317814.8:c.357C=	ENSP00000314774.4:p.Phe119=
ENST00000541682.6:c.372C=	ENSP00000446205.2:p.Phe124=
ENST00000577735.1:c.348C=	ENSP00000462491.1:p.Phe116=
NM_001165967.1:c.372C=	NP_001159439.1:p.Phe124=
NM_032580.3:c.357C=	NP_115969.2:p.Phe119=
XM_011524038.1:c.477C=	XP_011522340.1:p.Phe159=
XM_011524039.1:c.468C=	XP_011522341.1:p.Phe156=
XM_011524040.1:c.468C=	XP_011522342.1:p.Phe156=
XM_011524041.1:c.459C=	XP_011522343.1:p.Phe153=
XM_011524042.1:c.330C=	XP_011522344.1:p.Phe110=
XR_934203.1:n.69+2078G=
XM_017025232.1:c.477C=	XP_016880721.1:p.Phe159=
XM_024451007.1:c.477C=	XP_024306775.1:p.Phe159=
NM_001165967.2:c.372C= MANE Select	NP_001159439.1:p.Phe124=
NM_032580.4:c.357C=	NP_115969.2:p.Phe119=