Canonical Allele Identifier: CA2246160955

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122037G= , CM000679.2:g.8122037G=	GRCh38
NC_000017.10:g.8025355G= , CM000679.1:g.8025355G=	GRCh37
NC_000017.9:g.7966080G=	NCBI36
NG_015807.1:g.1880C=
NG_015816.1:g.7056C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.227C= MANE Select	ENSP00000446205.2:p.Ala76=
ENST00000317814.8:c.227-15C=	ENSP00000314774.4:n.227-15C=
ENST00000541682.6:c.227C=	ENSP00000446205.2:p.Ala76=
ENST00000577735.1:c.203C=	ENSP00000462491.1:p.Ala68=
NM_001165967.1:c.227C=	NP_001159439.1:p.Ala76=
NM_032580.3:c.227-15C=	NP_115969.2:n.227-15C=
XM_011524038.1:c.332C=	XP_011522340.1:p.Ala111=
XM_011524039.1:c.323C=	XP_011522341.1:p.Ala108=
XM_011524040.1:c.323C=	XP_011522342.1:p.Ala108=
XM_011524041.1:c.314C=	XP_011522343.1:p.Ala105=
XM_011524042.1:c.185C=	XP_011522344.1:p.Ala62=
XR_934203.1:n.69+2223G=
XM_017025232.1:c.332C=	XP_016880721.1:p.Ala111=
XM_024451007.1:c.332C=	XP_024306775.1:p.Ala111=
NM_001165967.2:c.227C= MANE Select	NP_001159439.1:p.Ala76=
NM_032580.4:c.227-15C=	NP_115969.2:n.227-15C=