Canonical Allele Identifier: CA2246160303

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121773T= , CM000679.2:g.8121773T=	GRCh38
NC_000017.10:g.8025091T= , CM000679.1:g.8025091T=	GRCh37
NC_000017.9:g.7965816T=	NCBI36
NG_015807.1:g.2144A=
NG_015816.1:g.7320A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000541682.7:c.491A= MANE Select	ENSP00000446205.2:p.His164=
ENST00000317814.8:c.476A=	ENSP00000314774.4:p.His159=
ENST00000541682.6:c.491A=	ENSP00000446205.2:p.His164=
NM_001165967.1:c.491A=	NP_001159439.1:p.His164=
NM_032580.3:c.476A=	NP_115969.2:p.His159=
XM_011524038.1:c.596A=	XP_011522340.1:p.His199=
XM_011524039.1:c.587A=	XP_011522341.1:p.His196=
XM_011524040.1:c.587A=	XP_011522342.1:p.His196=
XM_011524041.1:c.578A=	XP_011522343.1:p.His193=
XM_011524042.1:c.449A=	XP_011522344.1:p.His150=
XR_934203.1:n.69+1959T=
XM_017025232.1:c.596A=	XP_016880721.1:p.His199=
XM_024451007.1:c.596A=	XP_024306775.1:p.His199=
NM_001165967.2:c.491A= MANE Select	NP_001159439.1:p.His164=
NM_032580.4:c.476A=	NP_115969.2:p.His159=