Canonical Allele Identifier: CA397988215

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121845G>C , CM000679.2:g.8121845G>C	GRCh38
NC_000017.10:g.8025163G>C , CM000679.1:g.8025163G>C	GRCh37
NC_000017.9:g.7965888G>C	NCBI36
NG_015807.1:g.2072C>G
NG_015816.1:g.7248C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.419C>G MANE Select	ENSP00000446205.2:p.Pro140Arg
ENST00000317814.8:c.404C>G	ENSP00000314774.4:p.Pro135Arg
ENST00000541682.6:c.419C>G	ENSP00000446205.2:p.Pro140Arg
ENST00000577735.1:c.395C>G	ENSP00000462491.1:p.Pro132Arg
NM_001165967.1:c.419C>G	NP_001159439.1:p.Pro140Arg
NM_032580.3:c.404C>G	NP_115969.2:p.Pro135Arg
XM_011524038.1:c.524C>G	XP_011522340.1:p.Pro175Arg
XM_011524039.1:c.515C>G	XP_011522341.1:p.Pro172Arg
XM_011524040.1:c.515C>G	XP_011522342.1:p.Pro172Arg
XM_011524041.1:c.506C>G	XP_011522343.1:p.Pro169Arg
XM_011524042.1:c.377C>G	XP_011522344.1:p.Pro126Arg
XR_934203.1:n.69+2031G>C
XM_017025232.1:c.524C>G	XP_016880721.1:p.Pro175Arg
XM_024451007.1:c.524C>G	XP_024306775.1:p.Pro175Arg
NM_001165967.2:c.419C>G MANE Select	NP_001159439.1:p.Pro140Arg
NM_032580.4:c.404C>G	NP_115969.2:p.Pro135Arg