Canonical Allele Identifier: CA2808397536

Gene: HES7

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8122003del , CM000679.2:g.8122003del	GRCh38
NC_000017.10:g.8025321del , CM000679.1:g.8025321del	GRCh37
NC_000017.9:g.7966046del	NCBI36
NG_015807.1:g.1915del
NG_015816.1:g.7091del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541682.7:c.262del MANE Select	ENSP00000446205.2:p.Gln88ArgfsTer?
ENST00000317814.8:c.247del	ENSP00000314774.4:p.Gln83ArgfsTer?
ENST00000541682.6:c.262del	ENSP00000446205.2:p.Gln88ArgfsTer?
ENST00000577735.1:c.238del	ENSP00000462491.1:p.Gln80ArgfsTer?
NM_001165967.1:c.262del	NP_001159439.1:p.Gln88ArgfsTer?
NM_032580.3:c.247del	NP_115969.2:p.Gln83ArgfsTer?
XM_011524038.1:c.367del	XP_011522340.1:p.Gln123ArgfsTer?
XM_011524039.1:c.358del	XP_011522341.1:p.Gln120ArgfsTer?
XM_011524040.1:c.358del	XP_011522342.1:p.Gln120ArgfsTer?
XM_011524041.1:c.349del	XP_011522343.1:p.Gln117ArgfsTer?
XM_011524042.1:c.220del	XP_011522344.1:p.Gln74ArgfsTer?
XR_934203.1:n.69+2189del
XM_017025232.1:c.367del	XP_016880721.1:p.Gln123ArgfsTer?
XM_024451007.1:c.367del	XP_024306775.1:p.Gln123ArgfsTer?
NM_001165967.2:c.262del MANE Select	NP_001159439.1:p.Gln88ArgfsTer?
NM_032580.4:c.247del	NP_115969.2:p.Gln83ArgfsTer?