Canonical Allele Identifier: CA497955071

Gene: HES7

Linked Data

• dbSNP Id: rs1420505523
• gnomAD v2: 17-8025045-T-G
• gnomAD v4: 17-8121727-T-G
• MyVariant Identifiers: chr17:g.8025045T>G (hg19) ; chr17:g.8121727T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121727T>G , CM000679.2:g.8121727T>G	GRCh38
NC_000017.10:g.8025045T>G , CM000679.1:g.8025045T>G	GRCh37
NC_000017.9:g.7965770T>G	NCBI36
NG_015807.1:g.2190A>C
NG_015816.1:g.7366A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.537A>C MANE Select	ENSP00000446205.2:p.Ala179=
ENST00000317814.8:c.522A>C	ENSP00000314774.4:p.Ala174=
ENST00000541682.6:c.537A>C	ENSP00000446205.2:p.Ala179=
NM_001165967.1:c.537A>C	NP_001159439.1:p.Ala179=
NM_032580.3:c.522A>C	NP_115969.2:p.Ala174=
XM_011524038.1:c.642A>C	XP_011522340.1:p.Ala214=
XM_011524039.1:c.633A>C	XP_011522341.1:p.Ala211=
XM_011524040.1:c.633A>C	XP_011522342.1:p.Ala211=
XM_011524041.1:c.624A>C	XP_011522343.1:p.Ala208=
XM_011524042.1:c.495A>C	XP_011522344.1:p.Ala165=
XR_934203.1:n.69+1913T>G
XM_017025232.1:c.642A>C	XP_016880721.1:p.Ala214=
XM_024451007.1:c.642A>C	XP_024306775.1:p.Ala214=
NM_001165967.2:c.537A>C MANE Select	NP_001159439.1:p.Ala179=
NM_032580.4:c.522A>C	NP_115969.2:p.Ala174=