Canonical Allele Identifier: CA2808397534

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8121627_8121628insT , CM000679.2:g.8121627_8121628insT	GRCh38
NC_000017.10:g.8024945_8024946insT , CM000679.1:g.8024945_8024946insT	GRCh37
NC_000017.9:g.7965670_7965671insT	NCBI36
NG_015807.1:g.2289_2290insA
NG_015816.1:g.7465_7466insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.636_637insA MANE Select	ENSP00000446205.2:p.Gly213ArgfsTer?
ENST00000317814.8:c.621_622insA	ENSP00000314774.4:p.Gly208ArgfsTer?
ENST00000541682.6:c.636_637insA	ENSP00000446205.2:p.Gly213ArgfsTer?
NM_001165967.1:c.636_637insA	NP_001159439.1:p.Gly213ArgfsTer?
NM_032580.3:c.621_622insA	NP_115969.2:p.Gly208ArgfsTer?
XM_011524038.1:c.741_742insA	XP_011522340.1:p.Gly248ArgfsTer?
XM_011524039.1:c.732_733insA	XP_011522341.1:p.Gly245ArgfsTer?
XM_011524040.1:c.732_733insA	XP_011522342.1:p.Gly245ArgfsTer?
XM_011524041.1:c.723_724insA	XP_011522343.1:p.Gly242ArgfsTer?
XM_011524042.1:c.594_595insA	XP_011522344.1:p.Gly199ArgfsTer?
XR_934203.1:n.69+1813_69+1814insT
XM_017025232.1:c.741_742insA	XP_016880721.1:p.Gly248ArgfsTer?
XM_024451007.1:c.741_742insA	XP_024306775.1:p.Gly248ArgfsTer?
NM_001165967.2:c.636_637insA MANE Select	NP_001159439.1:p.Gly213ArgfsTer?
NM_032580.4:c.621_622insA	NP_115969.2:p.Gly208ArgfsTer?