Canonical Allele Identifier: CA2246160958

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122040G= , CM000679.2:g.8122040G=	GRCh38
NC_000017.10:g.8025358G= , CM000679.1:g.8025358G=	GRCh37
NC_000017.9:g.7966083G=	NCBI36
NG_015807.1:g.1877C=
NG_015816.1:g.7053C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.227-3C= MANE Select	ENSP00000446205.2:n.227-3C=
ENST00000317814.8:c.227-18C=	ENSP00000314774.4:n.227-18C=
ENST00000541682.6:c.227-3C=	ENSP00000446205.2:n.227-3C=
ENST00000577735.1:c.203-3C=	ENSP00000462491.1:n.203-3C=
NM_001165967.1:c.227-3C=	NP_001159439.1:n.227-3C=
NM_032580.3:c.227-18C=	NP_115969.2:n.227-18C=
XM_011524038.1:c.332-3C=	XP_011522340.1:n.332-3C=
XM_011524039.1:c.323-3C=	XP_011522341.1:n.323-3C=
XM_011524040.1:c.323-3C=	XP_011522342.1:n.323-3C=
XM_011524041.1:c.314-3C=	XP_011522343.1:n.314-3C=
XM_011524042.1:c.185-3C=	XP_011522344.1:n.185-3C=
XR_934203.1:n.69+2226G=
XM_017025232.1:c.332-3C=	XP_016880721.1:n.332-3C=
XM_024451007.1:c.332-3C=	XP_024306775.1:n.332-3C=
NM_001165967.2:c.227-3C= MANE Select	NP_001159439.1:n.227-3C=
NM_032580.4:c.227-18C=	NP_115969.2:n.227-18C=