Canonical Allele Identifier: CA1877946924

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377116_123377117delinsGA , CM000671.2:g.123377116_123377117delinsGA	GRCh38
NC_000009.11:g.126139395_126139396delinsGA , CM000671.1:g.126139395_126139396delinsGA	GRCh37
NC_000009.10:g.125179216_125179217delinsGA	NCBI36
NG_051311.1:g.28052_28053delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*54_*55delinsGA MANE Select	ENSP00000362734.3:n.*54_*55delinsGA
ENST00000373631.7:c.*54_*55delinsGA	ENSP00000362734.3:n.*54_*55delinsGA
ENST00000460253.1:c.*54_*55delinsGA	ENSP00000435279.1:n.*54_*55delinsGA
NM_173689.6:c.*54_*55delinsGA	NP_775960.4:n.*54_*55delinsGA
NR_104603.1:n.3026_3027delinsGA
XM_005251934.1:c.*54_*55delinsGA	XP_005251991.1:n.*54_*55delinsGA
XM_011518556.1:c.*54_*55delinsGA	XP_011516858.1:n.*54_*55delinsGA
XM_011518557.1:c.*54_*55delinsGA	XP_011516859.1:n.*54_*55delinsGA
XM_011518558.1:c.*54_*55delinsGA	XP_011516860.1:n.*54_*55delinsGA
XM_005251934.3:c.*54_*55delinsGA	XP_005251991.1:n.*54_*55delinsGA
XM_011518556.3:c.*54_*55delinsGA	XP_011516858.1:n.*54_*55delinsGA
XM_011518557.3:c.*54_*55delinsGA	XP_011516859.1:n.*54_*55delinsGA
XM_011518558.3:c.*54_*55delinsGA	XP_011516860.1:n.*54_*55delinsGA
NM_173689.7:c.*54_*55delinsGA MANE Select	NP_775960.4:n.*54_*55delinsGA
NR_104603.2:n.3026_3027delinsGA