Canonical Allele Identifier: CA497955423

Gene: HES7

Linked Data

• gnomAD v4: 17-8121871-C-T
• MyVariant Identifiers: chr17:g.8025189C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121871C>T , CM000679.2:g.8121871C>T	GRCh38
NC_000017.10:g.8025189C>T , CM000679.1:g.8025189C>T	GRCh37
NC_000017.9:g.7965914C>T	NCBI36
NG_015807.1:g.2046G>A
NG_015816.1:g.7222G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.393G>A MANE Select	ENSP00000446205.2:p.Leu131=
ENST00000317814.8:c.378G>A	ENSP00000314774.4:p.Leu126=
ENST00000541682.6:c.393G>A	ENSP00000446205.2:p.Leu131=
ENST00000577735.1:c.369G>A	ENSP00000462491.1:p.Leu123=
NM_001165967.1:c.393G>A	NP_001159439.1:p.Leu131=
NM_032580.3:c.378G>A	NP_115969.2:p.Leu126=
XM_011524038.1:c.498G>A	XP_011522340.1:p.Leu166=
XM_011524039.1:c.489G>A	XP_011522341.1:p.Leu163=
XM_011524040.1:c.489G>A	XP_011522342.1:p.Leu163=
XM_011524041.1:c.480G>A	XP_011522343.1:p.Leu160=
XM_011524042.1:c.351G>A	XP_011522344.1:p.Leu117=
XR_934203.1:n.69+2057C>T
XM_017025232.1:c.498G>A	XP_016880721.1:p.Leu166=
XM_024451007.1:c.498G>A	XP_024306775.1:p.Leu166=
NM_001165967.2:c.393G>A MANE Select	NP_001159439.1:p.Leu131=
NM_032580.4:c.378G>A	NP_115969.2:p.Leu126=