Canonical Allele Identifier: CA497955285

Gene: HES7

Linked Data

• MyVariant Identifiers: chr17:g.8025276G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121958G>A , CM000679.2:g.8121958G>A	GRCh38
NC_000017.10:g.8025276G>A , CM000679.1:g.8025276G>A	GRCh37
NC_000017.9:g.7966001G>A	NCBI36
NG_015807.1:g.1959C>T
NG_015816.1:g.7135C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.306C>T MANE Select	ENSP00000446205.2:p.Arg102=
ENST00000317814.8:c.291C>T	ENSP00000314774.4:p.Arg97=
ENST00000541682.6:c.306C>T	ENSP00000446205.2:p.Arg102=
ENST00000577735.1:c.282C>T	ENSP00000462491.1:p.Arg94=
NM_001165967.1:c.306C>T	NP_001159439.1:p.Arg102=
NM_032580.3:c.291C>T	NP_115969.2:p.Arg97=
XM_011524038.1:c.411C>T	XP_011522340.1:p.Arg137=
XM_011524039.1:c.402C>T	XP_011522341.1:p.Arg134=
XM_011524040.1:c.402C>T	XP_011522342.1:p.Arg134=
XM_011524041.1:c.393C>T	XP_011522343.1:p.Arg131=
XM_011524042.1:c.264C>T	XP_011522344.1:p.Arg88=
XR_934203.1:n.69+2144G>A
XM_017025232.1:c.411C>T	XP_016880721.1:p.Arg137=
XM_024451007.1:c.411C>T	XP_024306775.1:p.Arg137=
NM_001165967.2:c.306C>T MANE Select	NP_001159439.1:p.Arg102=
NM_032580.4:c.291C>T	NP_115969.2:p.Arg97=