Canonical Allele Identifier: CA2650261352

Gene: CR2

Linked Data

• gnomAD v4: 1-207454350-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454353del , CM000663.2:g.207454353del	GRCh38
NC_000001.10:g.207627698del , CM000663.1:g.207627698del	GRCh37
NC_000001.9:g.205694321del	NCBI36
NG_013006.1:g.5054del , LRG_348:g.5054del

Transcript Alleles

HGVS	Amino-acid change
ENST00000699640.1:c.-385+1258del	ENSP00000514493.1:n.-385+1258del
ENST00000367057.8:c.-66del MANE Select	ENSP00000356024.3:n.-66del
ENST00000367057.7:c.-66del	ENSP00000356024.3:n.-66del
ENST00000367058.7:c.-66del	ENSP00000356025.3:n.-66del
ENST00000367059.3:c.-66del	ENSP00000356026.3:n.-66del
NM_001006658.2:c.-66del , LRG_348t1:c.-66del	NP_001006659.1:n.-66del
NM_001877.4:c.-66del	NP_001868.2:n.-66del
NM_001006658.3:c.-66del MANE Select	NP_001006659.1:n.-66del
NM_001877.5:c.-66del	NP_001868.2:n.-66del