Canonical Allele Identifier: CA2246160072

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121692_8121693delinsTC , CM000679.2:g.8121692_8121693delinsTC	GRCh38
NC_000017.10:g.8025010_8025011delinsTC , CM000679.1:g.8025010_8025011delinsTC	GRCh37
NC_000017.9:g.7965735_7965736delinsTC	NCBI36
NG_015807.1:g.2224_2225delinsGA
NG_015816.1:g.7400_7401delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.571_572delinsGA MANE Select	ENSP00000446205.2:p.Asp191=
ENST00000317814.8:c.556_557delinsGA	ENSP00000314774.4:p.Asp186=
ENST00000541682.6:c.571_572delinsGA	ENSP00000446205.2:p.Asp191=
NM_001165967.1:c.571_572delinsGA	NP_001159439.1:p.Asp191=
NM_032580.3:c.556_557delinsGA	NP_115969.2:p.Asp186=
XM_011524038.1:c.676_677delinsGA	XP_011522340.1:p.Asp226=
XM_011524039.1:c.667_668delinsGA	XP_011522341.1:p.Asp223=
XM_011524040.1:c.667_668delinsGA	XP_011522342.1:p.Asp223=
XM_011524041.1:c.658_659delinsGA	XP_011522343.1:p.Asp220=
XM_011524042.1:c.529_530delinsGA	XP_011522344.1:p.Asp177=
XR_934203.1:n.69+1878_69+1879delinsTC
XM_017025232.1:c.676_677delinsGA	XP_016880721.1:p.Asp226=
XM_024451007.1:c.676_677delinsGA	XP_024306775.1:p.Asp226=
NM_001165967.2:c.571_572delinsGA MANE Select	NP_001159439.1:p.Asp191=
NM_032580.4:c.556_557delinsGA	NP_115969.2:p.Asp186=