Canonical Allele Identifier: CA1877946746

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377022_123377031delinsACAGTGTCCT , CM000671.2:g.123377022_123377031delinsACAGTGTCCT	GRCh38
NC_000009.11:g.126139301_126139310delinsACAGTGTCCT , CM000671.1:g.126139301_126139310delinsACAGTGTCCT	GRCh37
NC_000009.10:g.125179122_125179131delinsACAGTGTCCT	NCBI36
NG_051311.1:g.27958_27967delinsACAGTGTCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3818_3827delinsACAGTGTCCT MANE Select	ENSP00000362734.3:p.Asp1273=
ENST00000373631.7:c.3818_3827delinsACAGTGTCCT	ENSP00000362734.3:p.Asp1273=
ENST00000460253.1:c.2822_2831delinsACAGTGTCCT	ENSP00000435279.1:p.Asp941=
NM_173689.6:c.3818_3827delinsACAGTGTCCT	NP_775960.4:p.Asp1273=
NR_104603.1:n.2932_2941delinsACAGTGTCCT
XM_005251934.1:c.2822_2831delinsACAGTGTCCT	XP_005251991.1:p.Asp941=
XM_011518556.1:c.3791_3800delinsACAGTGTCCT	XP_011516858.1:p.Asp1264=
XM_011518557.1:c.3623_3632delinsACAGTGTCCT	XP_011516859.1:p.Asp1208=
XM_011518558.1:c.3623_3632delinsACAGTGTCCT	XP_011516860.1:p.Asp1208=
XM_005251934.3:c.2822_2831delinsACAGTGTCCT	XP_005251991.1:p.Asp941=
XM_011518556.3:c.3791_3800delinsACAGTGTCCT	XP_011516858.1:p.Asp1264=
XM_011518557.3:c.3623_3632delinsACAGTGTCCT	XP_011516859.1:p.Asp1208=
XM_011518558.3:c.3623_3632delinsACAGTGTCCT	XP_011516860.1:p.Asp1208=
NM_173689.7:c.3818_3827delinsACAGTGTCCT MANE Select	NP_775960.4:p.Asp1273=
NR_104603.2:n.2932_2941delinsACAGTGTCCT