Canonical Allele Identifier: CA2246160855

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121989_8121990delinsGC , CM000679.2:g.8121989_8121990delinsGC	GRCh38
NC_000017.10:g.8025307_8025308delinsGC , CM000679.1:g.8025307_8025308delinsGC	GRCh37
NC_000017.9:g.7966032_7966033delinsGC	NCBI36
NG_015807.1:g.1927_1928delinsGC
NG_015816.1:g.7103_7104delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.274_275delinsGC MANE Select	ENSP00000446205.2:p.Ala92=
ENST00000317814.8:c.259_260delinsGC	ENSP00000314774.4:p.Ala87=
ENST00000541682.6:c.274_275delinsGC	ENSP00000446205.2:p.Ala92=
ENST00000577735.1:c.250_251delinsGC	ENSP00000462491.1:p.Ala84=
NM_001165967.1:c.274_275delinsGC	NP_001159439.1:p.Ala92=
NM_032580.3:c.259_260delinsGC	NP_115969.2:p.Ala87=
XM_011524038.1:c.379_380delinsGC	XP_011522340.1:p.Ala127=
XM_011524039.1:c.370_371delinsGC	XP_011522341.1:p.Ala124=
XM_011524040.1:c.370_371delinsGC	XP_011522342.1:p.Ala124=
XM_011524041.1:c.361_362delinsGC	XP_011522343.1:p.Ala121=
XM_011524042.1:c.232_233delinsGC	XP_011522344.1:p.Ala78=
XR_934203.1:n.69+2175_69+2176delinsGC
XM_017025232.1:c.379_380delinsGC	XP_016880721.1:p.Ala127=
XM_024451007.1:c.379_380delinsGC	XP_024306775.1:p.Ala127=
NM_001165967.2:c.274_275delinsGC MANE Select	NP_001159439.1:p.Ala92=
NM_032580.4:c.259_260delinsGC	NP_115969.2:p.Ala87=