Canonical Allele Identifier: CA2246159721

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121551C= , CM000679.2:g.8121551C=	GRCh38
NC_000017.10:g.8024869C= , CM000679.1:g.8024869C=	GRCh37
NC_000017.9:g.7965594C=	NCBI36
NG_015807.1:g.2366G=
NG_015816.1:g.7542G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*20G= MANE Select	ENSP00000446205.2:n.*20G=
ENST00000541682.6:c.713G=	ENSP00000446205.2:n.713G=
NM_001165967.1:c.*20G=	NP_001159439.1:n.*20G=
NM_032580.3:c.*20G=	NP_115969.2:n.*20G=
XM_011524038.1:c.*20G=	XP_011522340.1:n.*20G=
XM_011524039.1:c.*20G=	XP_011522341.1:n.*20G=
XM_011524040.1:c.*20G=	XP_011522342.1:n.*20G=
XM_011524041.1:c.*20G=	XP_011522343.1:n.*20G=
XM_011524042.1:c.*20G=	XP_011522344.1:n.*20G=
XR_934203.1:n.69+1737C=
XM_017025232.1:c.*20G=	XP_016880721.1:n.*20G=
XM_024451007.1:c.*20G=	XP_024306775.1:n.*20G=
NM_001165967.2:c.*20G= MANE Select	NP_001159439.1:n.*20G=
NM_032580.4:c.*20G=	NP_115969.2:n.*20G=