Canonical Allele Identifier: CA2246159817

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121601_8121602delinsCG , CM000679.2:g.8121601_8121602delinsCG	GRCh38
NC_000017.10:g.8024919_8024920delinsCG , CM000679.1:g.8024919_8024920delinsCG	GRCh37
NC_000017.9:g.7965644_7965645delinsCG	NCBI36
NG_015807.1:g.2315_2316delinsCG
NG_015816.1:g.7491_7492delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.662_663delinsCG MANE Select	ENSP00000446205.2:p.Pro221=
ENST00000317814.8:c.647_648delinsCG	ENSP00000314774.4:p.Pro216=
ENST00000541682.6:c.662_663delinsCG	ENSP00000446205.2:p.Pro221=
NM_001165967.1:c.662_663delinsCG	NP_001159439.1:p.Pro221=
NM_032580.3:c.647_648delinsCG	NP_115969.2:p.Pro216=
XM_011524038.1:c.767_768delinsCG	XP_011522340.1:p.Pro256=
XM_011524039.1:c.758_759delinsCG	XP_011522341.1:p.Pro253=
XM_011524040.1:c.758_759delinsCG	XP_011522342.1:p.Pro253=
XM_011524041.1:c.749_750delinsCG	XP_011522343.1:p.Pro250=
XM_011524042.1:c.620_621delinsCG	XP_011522344.1:p.Pro207=
XR_934203.1:n.69+1787_69+1788delinsCG
XM_017025232.1:c.767_768delinsCG	XP_016880721.1:p.Pro256=
XM_024451007.1:c.767_768delinsCG	XP_024306775.1:p.Pro256=
NM_001165967.2:c.662_663delinsCG MANE Select	NP_001159439.1:p.Pro221=
NM_032580.4:c.647_648delinsCG	NP_115969.2:p.Pro216=