Canonical Allele Identifier: CA2246158040

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8120791A= , CM000679.2:g.8120791A=	GRCh38
NC_000017.10:g.8024109A= , CM000679.1:g.8024109A=	GRCh37
NC_000017.9:g.7964834A=	NCBI36
NG_015807.1:g.3126T=
NG_015816.1:g.8302T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*780T= MANE Select	ENSP00000446205.2:n.*780T=
ENST00000541682.6:c.1473T=	ENSP00000446205.2:n.1473T=
NM_001165967.1:c.*780T=	NP_001159439.1:n.*780T=
NM_032580.3:c.*780T=	NP_115969.2:n.*780T=
XM_011524038.1:c.*780T=	XP_011522340.1:n.*780T=
XR_934203.1:n.69+977A=
XM_017025232.1:c.*780T=	XP_016880721.1:n.*780T=
XM_024451007.1:c.*780T=	XP_024306775.1:n.*780T=
NM_001165967.2:c.*780T= MANE Select	NP_001159439.1:n.*780T=
NM_032580.4:c.*780T=	NP_115969.2:n.*780T=