Canonical Allele Identifier: CA497955432

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025332G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122014G>T , CM000679.2:g.8122014G>T	GRCh38
NC_000017.10:g.8025332G>T , CM000679.1:g.8025332G>T	GRCh37
NC_000017.9:g.7966057G>T	NCBI36
NG_015807.1:g.1903C>A
NG_015816.1:g.7079C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.250C>A MANE Select	ENSP00000446205.2:p.Arg84=
ENST00000317814.8:c.235C>A	ENSP00000314774.4:p.Arg79=
ENST00000541682.6:c.250C>A	ENSP00000446205.2:p.Arg84=
ENST00000577735.1:c.226C>A	ENSP00000462491.1:p.Arg76=
NM_001165967.1:c.250C>A	NP_001159439.1:p.Arg84=
NM_032580.3:c.235C>A	NP_115969.2:p.Arg79=
XM_011524038.1:c.355C>A	XP_011522340.1:p.Arg119=
XM_011524039.1:c.346C>A	XP_011522341.1:p.Arg116=
XM_011524040.1:c.346C>A	XP_011522342.1:p.Arg116=
XM_011524041.1:c.337C>A	XP_011522343.1:p.Arg113=
XM_011524042.1:c.208C>A	XP_011522344.1:p.Arg70=
XR_934203.1:n.69+2200G>T
XM_017025232.1:c.355C>A	XP_016880721.1:p.Arg119=
XM_024451007.1:c.355C>A	XP_024306775.1:p.Arg119=
NM_001165967.2:c.250C>A MANE Select	NP_001159439.1:p.Arg84=
NM_032580.4:c.235C>A	NP_115969.2:p.Arg79=