Canonical Allele Identifier: CA397988713

Gene: HES7

Linked Data

• gnomAD v4: 17-8121957-C-G
• MyVariant Identifiers: chr17:g.8025275C>G (hg19) ; chr17:g.8121957C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121957C>G , CM000679.2:g.8121957C>G	GRCh38
NC_000017.10:g.8025275C>G , CM000679.1:g.8025275C>G	GRCh37
NC_000017.9:g.7966000C>G	NCBI36
NG_015807.1:g.1960G>C
NG_015816.1:g.7136G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.307G>C MANE Select	ENSP00000446205.2:p.Glu103Gln
ENST00000317814.8:c.292G>C	ENSP00000314774.4:p.Glu98Gln
ENST00000541682.6:c.307G>C	ENSP00000446205.2:p.Glu103Gln
ENST00000577735.1:c.283G>C	ENSP00000462491.1:p.Glu95Gln
NM_001165967.1:c.307G>C	NP_001159439.1:p.Glu103Gln
NM_032580.3:c.292G>C	NP_115969.2:p.Glu98Gln
XM_011524038.1:c.412G>C	XP_011522340.1:p.Glu138Gln
XM_011524039.1:c.403G>C	XP_011522341.1:p.Glu135Gln
XM_011524040.1:c.403G>C	XP_011522342.1:p.Glu135Gln
XM_011524041.1:c.394G>C	XP_011522343.1:p.Glu132Gln
XM_011524042.1:c.265G>C	XP_011522344.1:p.Glu89Gln
XR_934203.1:n.69+2143C>G
XM_017025232.1:c.412G>C	XP_016880721.1:p.Glu138Gln
XM_024451007.1:c.412G>C	XP_024306775.1:p.Glu138Gln
NM_001165967.2:c.307G>C MANE Select	NP_001159439.1:p.Glu103Gln
NM_032580.4:c.292G>C	NP_115969.2:p.Glu98Gln