Canonical Allele Identifier: CA397988899

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025309C>G (hg19) ; chr17:g.8121991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121991C>G , CM000679.2:g.8121991C>G	GRCh38
NC_000017.10:g.8025309C>G , CM000679.1:g.8025309C>G	GRCh37
NC_000017.9:g.7966034C>G	NCBI36
NG_015807.1:g.1926G>C
NG_015816.1:g.7102G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.273G>C MANE Select	ENSP00000446205.2:p.Glu91Asp
ENST00000317814.8:c.258G>C	ENSP00000314774.4:p.Glu86Asp
ENST00000541682.6:c.273G>C	ENSP00000446205.2:p.Glu91Asp
ENST00000577735.1:c.249G>C	ENSP00000462491.1:p.Glu83Asp
NM_001165967.1:c.273G>C	NP_001159439.1:p.Glu91Asp
NM_032580.3:c.258G>C	NP_115969.2:p.Glu86Asp
XM_011524038.1:c.378G>C	XP_011522340.1:p.Glu126Asp
XM_011524039.1:c.369G>C	XP_011522341.1:p.Glu123Asp
XM_011524040.1:c.369G>C	XP_011522342.1:p.Glu123Asp
XM_011524041.1:c.360G>C	XP_011522343.1:p.Glu120Asp
XM_011524042.1:c.231G>C	XP_011522344.1:p.Glu77Asp
XR_934203.1:n.69+2177C>G
XM_017025232.1:c.378G>C	XP_016880721.1:p.Glu126Asp
XM_024451007.1:c.378G>C	XP_024306775.1:p.Glu126Asp
NM_001165967.2:c.273G>C MANE Select	NP_001159439.1:p.Glu91Asp
NM_032580.4:c.258G>C	NP_115969.2:p.Glu86Asp