Canonical Allele Identifier: CA397987217

Gene: HES7

Linked Data

• gnomAD v4: 17-8121650-G-T
• MyVariant Identifiers: chr17:g.8024968G>T (hg19) ; chr17:g.8121650G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121650G>T , CM000679.2:g.8121650G>T	GRCh38
NC_000017.10:g.8024968G>T , CM000679.1:g.8024968G>T	GRCh37
NC_000017.9:g.7965693G>T	NCBI36
NG_015807.1:g.2267C>A
NG_015816.1:g.7443C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.614C>A MANE Select	ENSP00000446205.2:p.Pro205Gln
ENST00000317814.8:c.599C>A	ENSP00000314774.4:p.Pro200Gln
ENST00000541682.6:c.614C>A	ENSP00000446205.2:p.Pro205Gln
NM_001165967.1:c.614C>A	NP_001159439.1:p.Pro205Gln
NM_032580.3:c.599C>A	NP_115969.2:p.Pro200Gln
XM_011524038.1:c.719C>A	XP_011522340.1:p.Pro240Gln
XM_011524039.1:c.710C>A	XP_011522341.1:p.Pro237Gln
XM_011524040.1:c.710C>A	XP_011522342.1:p.Pro237Gln
XM_011524041.1:c.701C>A	XP_011522343.1:p.Pro234Gln
XM_011524042.1:c.572C>A	XP_011522344.1:p.Pro191Gln
XR_934203.1:n.69+1836G>T
XM_017025232.1:c.719C>A	XP_016880721.1:p.Pro240Gln
XM_024451007.1:c.719C>A	XP_024306775.1:p.Pro240Gln
NM_001165967.2:c.614C>A MANE Select	NP_001159439.1:p.Pro205Gln
NM_032580.4:c.599C>A	NP_115969.2:p.Pro200Gln