Canonical Allele Identifier: CA1877946341

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123376849_123376855delinsCCTGCCG , CM000671.2:g.123376849_123376855delinsCCTGCCG	GRCh38
NC_000009.11:g.126139128_126139134delinsCCTGCCG , CM000671.1:g.126139128_126139134delinsCCTGCCG	GRCh37
NC_000009.10:g.125178949_125178955delinsCCTGCCG	NCBI36
NG_051311.1:g.27785_27791delinsCCTGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.3645_3651delinsCCTGCCG MANE Select	ENSP00000362734.3:p.Pro1215=
ENST00000373631.7:c.3645_3651delinsCCTGCCG	ENSP00000362734.3:p.Pro1215=
ENST00000460253.1:c.2649_2655delinsCCTGCCG	ENSP00000435279.1:p.Pro883=
NM_173689.6:c.3645_3651delinsCCTGCCG	NP_775960.4:p.Pro1215=
NR_104603.1:n.2759_2765delinsCCTGCCG
XM_005251934.1:c.2649_2655delinsCCTGCCG	XP_005251991.1:p.Pro883=
XM_011518556.1:c.3618_3624delinsCCTGCCG	XP_011516858.1:p.Pro1206=
XM_011518557.1:c.3450_3456delinsCCTGCCG	XP_011516859.1:p.Pro1150=
XM_011518558.1:c.3450_3456delinsCCTGCCG	XP_011516860.1:p.Pro1150=
XM_005251934.3:c.2649_2655delinsCCTGCCG	XP_005251991.1:p.Pro883=
XM_011518556.3:c.3618_3624delinsCCTGCCG	XP_011516858.1:p.Pro1206=
XM_011518557.3:c.3450_3456delinsCCTGCCG	XP_011516859.1:p.Pro1150=
XM_011518558.3:c.3450_3456delinsCCTGCCG	XP_011516860.1:p.Pro1150=
NM_173689.7:c.3645_3651delinsCCTGCCG MANE Select	NP_775960.4:p.Pro1215=
NR_104603.2:n.2759_2765delinsCCTGCCG