Canonical Allele Identifier: CA397988402

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025200G>C (hg19) ; chr17:g.8121882G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121882G>C , CM000679.2:g.8121882G>C	GRCh38
NC_000017.10:g.8025200G>C , CM000679.1:g.8025200G>C	GRCh37
NC_000017.9:g.7965925G>C	NCBI36
NG_015807.1:g.2035C>G
NG_015816.1:g.7211C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.382C>G MANE Select	ENSP00000446205.2:p.His128Asp
ENST00000317814.8:c.367C>G	ENSP00000314774.4:p.His123Asp
ENST00000541682.6:c.382C>G	ENSP00000446205.2:p.His128Asp
ENST00000577735.1:c.358C>G	ENSP00000462491.1:p.His120Asp
NM_001165967.1:c.382C>G	NP_001159439.1:p.His128Asp
NM_032580.3:c.367C>G	NP_115969.2:p.His123Asp
XM_011524038.1:c.487C>G	XP_011522340.1:p.His163Asp
XM_011524039.1:c.478C>G	XP_011522341.1:p.His160Asp
XM_011524040.1:c.478C>G	XP_011522342.1:p.His160Asp
XM_011524041.1:c.469C>G	XP_011522343.1:p.His157Asp
XM_011524042.1:c.340C>G	XP_011522344.1:p.His114Asp
XR_934203.1:n.69+2068G>C
XM_017025232.1:c.487C>G	XP_016880721.1:p.His163Asp
XM_024451007.1:c.487C>G	XP_024306775.1:p.His163Asp
NM_001165967.2:c.382C>G MANE Select	NP_001159439.1:p.His128Asp
NM_032580.4:c.367C>G	NP_115969.2:p.His123Asp