Canonical Allele Identifier: CA1877946811

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377047_123377051delinsGGAGA , CM000671.2:g.123377047_123377051delinsGGAGA	GRCh38
NC_000009.11:g.126139326_126139330delinsGGAGA , CM000671.1:g.126139326_126139330delinsGGAGA	GRCh37
NC_000009.10:g.125179147_125179151delinsGGAGA	NCBI36
NG_051311.1:g.27983_27987delinsGGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3843_3847delinsGGAGA MANE Select	ENSP00000362734.3:p.Glu1281=
ENST00000373631.7:c.3843_3847delinsGGAGA	ENSP00000362734.3:p.Glu1281=
ENST00000460253.1:c.2847_2851delinsGGAGA	ENSP00000435279.1:p.Glu949=
NM_173689.6:c.3843_3847delinsGGAGA	NP_775960.4:p.Glu1281=
NR_104603.1:n.2957_2961delinsGGAGA
XM_005251934.1:c.2847_2851delinsGGAGA	XP_005251991.1:p.Glu949=
XM_011518556.1:c.3816_3820delinsGGAGA	XP_011516858.1:p.Glu1272=
XM_011518557.1:c.3648_3652delinsGGAGA	XP_011516859.1:p.Glu1216=
XM_011518558.1:c.3648_3652delinsGGAGA	XP_011516860.1:p.Glu1216=
XM_005251934.3:c.2847_2851delinsGGAGA	XP_005251991.1:p.Glu949=
XM_011518556.3:c.3816_3820delinsGGAGA	XP_011516858.1:p.Glu1272=
XM_011518557.3:c.3648_3652delinsGGAGA	XP_011516859.1:p.Glu1216=
XM_011518558.3:c.3648_3652delinsGGAGA	XP_011516860.1:p.Glu1216=
NM_173689.7:c.3843_3847delinsGGAGA MANE Select	NP_775960.4:p.Glu1281=
NR_104603.2:n.2957_2961delinsGGAGA