Canonical Allele Identifier: CA2246160934

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122027A= , CM000679.2:g.8122027A=	GRCh38
NC_000017.10:g.8025345A= , CM000679.1:g.8025345A=	GRCh37
NC_000017.9:g.7966070A=	NCBI36
NG_015807.1:g.1890T=
NG_015816.1:g.7066T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.237T= MANE Select	ENSP00000446205.2:p.Ala79=
ENST00000317814.8:c.227-5T=	ENSP00000314774.4:n.227-5T=
ENST00000541682.6:c.237T=	ENSP00000446205.2:p.Ala79=
ENST00000577735.1:c.213T=	ENSP00000462491.1:p.Ala71=
NM_001165967.1:c.237T=	NP_001159439.1:p.Ala79=
NM_032580.3:c.227-5T=	NP_115969.2:n.227-5T=
XM_011524038.1:c.342T=	XP_011522340.1:p.Ala114=
XM_011524039.1:c.333T=	XP_011522341.1:p.Ala111=
XM_011524040.1:c.333T=	XP_011522342.1:p.Ala111=
XM_011524041.1:c.324T=	XP_011522343.1:p.Ala108=
XM_011524042.1:c.195T=	XP_011522344.1:p.Ala65=
XR_934203.1:n.69+2213A=
XM_017025232.1:c.342T=	XP_016880721.1:p.Ala114=
XM_024451007.1:c.342T=	XP_024306775.1:p.Ala114=
NM_001165967.2:c.237T= MANE Select	NP_001159439.1:p.Ala79=
NM_032580.4:c.227-5T=	NP_115969.2:n.227-5T=