Canonical Allele Identifier: CA397986934

Gene: HES7

Linked Data

• gnomAD v4: 17-8121594-C-A
• MyVariant Identifiers: chr17:g.8024912C>A (hg19) ; chr17:g.8121594C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121594C>A , CM000679.2:g.8121594C>A	GRCh38
NC_000017.10:g.8024912C>A , CM000679.1:g.8024912C>A	GRCh37
NC_000017.9:g.7965637C>A	NCBI36
NG_015807.1:g.2323G>T
NG_015816.1:g.7499G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.670G>T MANE Select	ENSP00000446205.2:p.Ala224Ser
ENST00000317814.8:c.655G>T	ENSP00000314774.4:p.Ala219Ser
ENST00000541682.6:c.670G>T	ENSP00000446205.2:p.Ala224Ser
NM_001165967.1:c.670G>T	NP_001159439.1:p.Ala224Ser
NM_032580.3:c.655G>T	NP_115969.2:p.Ala219Ser
XM_011524038.1:c.775G>T	XP_011522340.1:p.Ala259Ser
XM_011524039.1:c.766G>T	XP_011522341.1:p.Ala256Ser
XM_011524040.1:c.766G>T	XP_011522342.1:p.Ala256Ser
XM_011524041.1:c.757G>T	XP_011522343.1:p.Ala253Ser
XM_011524042.1:c.628G>T	XP_011522344.1:p.Ala210Ser
XR_934203.1:n.69+1780C>A
XM_017025232.1:c.775G>T	XP_016880721.1:p.Ala259Ser
XM_024451007.1:c.775G>T	XP_024306775.1:p.Ala259Ser
NM_001165967.2:c.670G>T MANE Select	NP_001159439.1:p.Ala224Ser
NM_032580.4:c.655G>T	NP_115969.2:p.Ala219Ser