Canonical Allele Identifier: CA497760783

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8024903T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121585T>G , CM000679.2:g.8121585T>G	GRCh38
NC_000017.10:g.8024903T>G , CM000679.1:g.8024903T>G	GRCh37
NC_000017.9:g.7965628T>G	NCBI36
NG_015807.1:g.2332A>C
NG_015816.1:g.7508A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.679A>C MANE Select	ENSP00000446205.2:p.Arg227=
ENST00000317814.8:c.664A>C	ENSP00000314774.4:p.Arg222=
ENST00000541682.6:c.679A>C	ENSP00000446205.2:p.Arg227=
NM_001165967.1:c.679A>C	NP_001159439.1:p.Arg227=
NM_032580.3:c.664A>C	NP_115969.2:p.Arg222=
XM_011524038.1:c.784A>C	XP_011522340.1:p.Arg262=
XM_011524039.1:c.775A>C	XP_011522341.1:p.Arg259=
XM_011524040.1:c.775A>C	XP_011522342.1:p.Arg259=
XM_011524041.1:c.766A>C	XP_011522343.1:p.Arg256=
XM_011524042.1:c.637A>C	XP_011522344.1:p.Arg213=
XR_934203.1:n.69+1771T>G
XM_017025232.1:c.784A>C	XP_016880721.1:p.Arg262=
XM_024451007.1:c.784A>C	XP_024306775.1:p.Arg262=
NM_001165967.2:c.679A>C MANE Select	NP_001159439.1:p.Arg227=
NM_032580.4:c.664A>C	NP_115969.2:p.Arg222=