Canonical Allele Identifier: CA397986918

Gene: HES7

Linked Data

• gnomAD v4: 17-8121590-A-G
• MyVariant Identifiers: chr17:g.8024908A>G (hg19) ; chr17:g.8121590A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121590A>G , CM000679.2:g.8121590A>G	GRCh38
NC_000017.10:g.8024908A>G , CM000679.1:g.8024908A>G	GRCh37
NC_000017.9:g.7965633A>G	NCBI36
NG_015807.1:g.2327T>C
NG_015816.1:g.7503T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.674T>C MANE Select	ENSP00000446205.2:p.Phe225Ser
ENST00000317814.8:c.659T>C	ENSP00000314774.4:p.Phe220Ser
ENST00000541682.6:c.674T>C	ENSP00000446205.2:p.Phe225Ser
NM_001165967.1:c.674T>C	NP_001159439.1:p.Phe225Ser
NM_032580.3:c.659T>C	NP_115969.2:p.Phe220Ser
XM_011524038.1:c.779T>C	XP_011522340.1:p.Phe260Ser
XM_011524039.1:c.770T>C	XP_011522341.1:p.Phe257Ser
XM_011524040.1:c.770T>C	XP_011522342.1:p.Phe257Ser
XM_011524041.1:c.761T>C	XP_011522343.1:p.Phe254Ser
XM_011524042.1:c.632T>C	XP_011522344.1:p.Phe211Ser
XR_934203.1:n.69+1776A>G
XM_017025232.1:c.779T>C	XP_016880721.1:p.Phe260Ser
XM_024451007.1:c.779T>C	XP_024306775.1:p.Phe260Ser
NM_001165967.2:c.674T>C MANE Select	NP_001159439.1:p.Phe225Ser
NM_032580.4:c.659T>C	NP_115969.2:p.Phe220Ser