Canonical Allele Identifier: CA497955492

Gene: HES7

Linked Data

• gnomAD v4: 17-8121913-C-A
• MyVariant Identifiers: chr17:g.8025231C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121913C>A , CM000679.2:g.8121913C>A	GRCh38
NC_000017.10:g.8025231C>A , CM000679.1:g.8025231C>A	GRCh37
NC_000017.9:g.7965956C>A	NCBI36
NG_015807.1:g.2004G>T
NG_015816.1:g.7180G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.351G>T MANE Select	ENSP00000446205.2:p.Pro117=
ENST00000317814.8:c.336G>T	ENSP00000314774.4:p.Pro112=
ENST00000541682.6:c.351G>T	ENSP00000446205.2:p.Pro117=
ENST00000577735.1:c.327G>T	ENSP00000462491.1:p.Pro109=
NM_001165967.1:c.351G>T	NP_001159439.1:p.Pro117=
NM_032580.3:c.336G>T	NP_115969.2:p.Pro112=
XM_011524038.1:c.456G>T	XP_011522340.1:p.Pro152=
XM_011524039.1:c.447G>T	XP_011522341.1:p.Pro149=
XM_011524040.1:c.447G>T	XP_011522342.1:p.Pro149=
XM_011524041.1:c.438G>T	XP_011522343.1:p.Pro146=
XM_011524042.1:c.309G>T	XP_011522344.1:p.Pro103=
XR_934203.1:n.69+2099C>A
XM_017025232.1:c.456G>T	XP_016880721.1:p.Pro152=
XM_024451007.1:c.456G>T	XP_024306775.1:p.Pro152=
NM_001165967.2:c.351G>T MANE Select	NP_001159439.1:p.Pro117=
NM_032580.4:c.336G>T	NP_115969.2:p.Pro112=