Canonical Allele Identifier: CA2635936576

Gene: HES7

Linked Data

• gnomAD v4: 17-8121566-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121566A>G , CM000679.2:g.8121566A>G	GRCh38
NC_000017.10:g.8024884A>G , CM000679.1:g.8024884A>G	GRCh37
NC_000017.9:g.7965609A>G	NCBI36
NG_015807.1:g.2351T>C
NG_015816.1:g.7527T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.*5T>C MANE Select	ENSP00000446205.2:n.*5T>C
ENST00000541682.6:c.698T>C	ENSP00000446205.2:n.698T>C
NM_001165967.1:c.*5T>C	NP_001159439.1:n.*5T>C
NM_032580.3:c.*5T>C	NP_115969.2:n.*5T>C
XM_011524038.1:c.*5T>C	XP_011522340.1:n.*5T>C
XM_011524039.1:c.*5T>C	XP_011522341.1:n.*5T>C
XM_011524040.1:c.*5T>C	XP_011522342.1:n.*5T>C
XM_011524041.1:c.*5T>C	XP_011522343.1:n.*5T>C
XM_011524042.1:c.*5T>C	XP_011522344.1:n.*5T>C
XR_934203.1:n.69+1752A>G
XM_017025232.1:c.*5T>C	XP_016880721.1:n.*5T>C
XM_024451007.1:c.*5T>C	XP_024306775.1:n.*5T>C
NM_001165967.2:c.*5T>C MANE Select	NP_001159439.1:n.*5T>C
NM_032580.4:c.*5T>C	NP_115969.2:n.*5T>C