Canonical Allele Identifier: CA2635934683

Gene: HES7

Linked Data

• gnomAD v4: 17-8120804-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8120804T>A , CM000679.2:g.8120804T>A	GRCh38
NC_000017.10:g.8024122T>A , CM000679.1:g.8024122T>A	GRCh37
NC_000017.9:g.7964847T>A	NCBI36
NG_015807.1:g.3113A>T
NG_015816.1:g.8289A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000541682.7:c.*767A>T MANE Select	ENSP00000446205.2:n.*767A>T
ENST00000541682.6:c.1460A>T	ENSP00000446205.2:n.1460A>T
NM_001165967.1:c.*767A>T	NP_001159439.1:n.*767A>T
NM_032580.3:c.*767A>T	NP_115969.2:n.*767A>T
XM_011524038.1:c.*767A>T	XP_011522340.1:n.*767A>T
XR_934203.1:n.69+990T>A
XM_017025232.1:c.*767A>T	XP_016880721.1:n.*767A>T
XM_024451007.1:c.*767A>T	XP_024306775.1:n.*767A>T
NM_001165967.2:c.*767A>T MANE Select	NP_001159439.1:n.*767A>T
NM_032580.4:c.*767A>T	NP_115969.2:n.*767A>T