Canonical Allele Identifier: CA2246160790

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121964_8121965delinsAC , CM000679.2:g.8121964_8121965delinsAC	GRCh38
NC_000017.10:g.8025282_8025283delinsAC , CM000679.1:g.8025282_8025283delinsAC	GRCh37
NC_000017.9:g.7966007_7966008delinsAC	NCBI36
NG_015807.1:g.1952_1953delinsGT
NG_015816.1:g.7128_7129delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.299_300delinsGT MANE Select	ENSP00000446205.2:p.Gly100=
ENST00000317814.8:c.284_285delinsGT	ENSP00000314774.4:p.Gly95=
ENST00000541682.6:c.299_300delinsGT	ENSP00000446205.2:p.Gly100=
ENST00000577735.1:c.275_276delinsGT	ENSP00000462491.1:p.Gly92=
NM_001165967.1:c.299_300delinsGT	NP_001159439.1:p.Gly100=
NM_032580.3:c.284_285delinsGT	NP_115969.2:p.Gly95=
XM_011524038.1:c.404_405delinsGT	XP_011522340.1:p.Gly135=
XM_011524039.1:c.395_396delinsGT	XP_011522341.1:p.Gly132=
XM_011524040.1:c.395_396delinsGT	XP_011522342.1:p.Gly132=
XM_011524041.1:c.386_387delinsGT	XP_011522343.1:p.Gly129=
XM_011524042.1:c.257_258delinsGT	XP_011522344.1:p.Gly86=
XR_934203.1:n.69+2150_69+2151delinsAC
XM_017025232.1:c.404_405delinsGT	XP_016880721.1:p.Gly135=
XM_024451007.1:c.404_405delinsGT	XP_024306775.1:p.Gly135=
NM_001165967.2:c.299_300delinsGT MANE Select	NP_001159439.1:p.Gly100=
NM_032580.4:c.284_285delinsGT	NP_115969.2:p.Gly95=