Canonical Allele Identifier: CA2635934707

Gene: HES7

Linked Data

• gnomAD v4: 17-8120818-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8120818C>A , CM000679.2:g.8120818C>A	GRCh38
NC_000017.10:g.8024136C>A , CM000679.1:g.8024136C>A	GRCh37
NC_000017.9:g.7964861C>A	NCBI36
NG_015807.1:g.3099G>T
NG_015816.1:g.8275G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000541682.7:c.*753G>T MANE Select	ENSP00000446205.2:n.*753G>T
ENST00000541682.6:c.1446G>T	ENSP00000446205.2:n.1446G>T
NM_001165967.1:c.*753G>T	NP_001159439.1:n.*753G>T
NM_032580.3:c.*753G>T	NP_115969.2:n.*753G>T
XM_011524038.1:c.*753G>T	XP_011522340.1:n.*753G>T
XR_934203.1:n.69+1004C>A
XM_017025232.1:c.*753G>T	XP_016880721.1:n.*753G>T
XM_024451007.1:c.*753G>T	XP_024306775.1:n.*753G>T
NM_001165967.2:c.*753G>T MANE Select	NP_001159439.1:n.*753G>T
NM_032580.4:c.*753G>T	NP_115969.2:n.*753G>T