Canonical Allele Identifier: CA2650261408
Gene: CR2 HGNC NCBI

Linked Data

gnomAD v4: 1-207454400-CG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454405del , CM000663.2:g.207454405del GRCh38
NC_000001.10:g.207627750del , CM000663.1:g.207627750del GRCh37
NC_000001.9:g.205694373del NCBI36
NG_013006.1:g.5106del , LRG_348:g.5106del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-456del ENSP00000514480.1:n.-456del
ENST00000699640.1:c.-385+1310del ENSP00000514493.1:n.-385+1310del
ENST00000367057.8:c.-14del MANE Select ENSP00000356024.3:n.-14del
ENST00000367057.7:c.-14del ENSP00000356024.3:n.-14del
ENST00000367058.7:c.-14del ENSP00000356025.3:n.-14del
ENST00000367059.3:c.-14del ENSP00000356026.3:n.-14del
NM_001006658.2:c.-14del , LRG_348t1:c.-14del NP_001006659.1:n.-14del
NM_001877.4:c.-14del NP_001868.2:n.-14del
NM_001006658.3:c.-14del MANE Select NP_001006659.1:n.-14del
NM_001877.5:c.-14del NP_001868.2:n.-14del
Search 100 bp 5'
Search 100 bp 3'