Canonical Allele Identifier: CA1877946873

Gene: CRB2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123377087_123377141delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG , CM000671.2:g.123377087_123377141delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	GRCh38
NC_000009.11:g.126139366_126139420delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG , CM000671.1:g.126139366_126139420delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	GRCh37
NC_000009.10:g.125179187_125179241delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	NCBI36
NG_051311.1:g.28023_28077delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373631.8:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG MANE Select	ENSP00000362734.3:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCT...
ENST00000373631.7:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	ENSP00000362734.3:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCT...
ENST00000460253.1:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	ENSP00000435279.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCT...
NM_173689.6:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	NP_775960.4:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGAC...
NR_104603.1:n.2997_3051delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG
XM_005251934.1:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_005251991.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
XM_011518556.1:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_011516858.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
XM_011518557.1:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_011516859.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
XM_011518558.1:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_011516860.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
XM_005251934.3:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_005251991.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
XM_011518556.3:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_011516858.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
XM_011518557.3:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_011516859.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
XM_011518558.3:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG	XP_011516860.1:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGA...
NM_173689.7:c.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG MANE Select	NP_775960.4:n.*25_*79delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGAC...
NR_104603.2:n.2997_3051delinsACCTGGAGGTCCTGAATGGTTTCTACCTGGAGACCCAAGGAAGCTGCTTCCAGGG