Canonical Allele Identifier: CA2246160945

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122031G= , CM000679.2:g.8122031G=	GRCh38
NC_000017.10:g.8025349G= , CM000679.1:g.8025349G=	GRCh37
NC_000017.9:g.7966074G=	NCBI36
NG_015807.1:g.1886C=
NG_015816.1:g.7062C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.233C= MANE Select	ENSP00000446205.2:p.Ala78=
ENST00000317814.8:c.227-9C=	ENSP00000314774.4:n.227-9C=
ENST00000541682.6:c.233C=	ENSP00000446205.2:p.Ala78=
ENST00000577735.1:c.209C=	ENSP00000462491.1:p.Ala70=
NM_001165967.1:c.233C=	NP_001159439.1:p.Ala78=
NM_032580.3:c.227-9C=	NP_115969.2:n.227-9C=
XM_011524038.1:c.338C=	XP_011522340.1:p.Ala113=
XM_011524039.1:c.329C=	XP_011522341.1:p.Ala110=
XM_011524040.1:c.329C=	XP_011522342.1:p.Ala110=
XM_011524041.1:c.320C=	XP_011522343.1:p.Ala107=
XM_011524042.1:c.191C=	XP_011522344.1:p.Ala64=
XR_934203.1:n.69+2217G=
XM_017025232.1:c.338C=	XP_016880721.1:p.Ala113=
XM_024451007.1:c.338C=	XP_024306775.1:p.Ala113=
NM_001165967.2:c.233C= MANE Select	NP_001159439.1:p.Ala78=
NM_032580.4:c.227-9C=	NP_115969.2:n.227-9C=