Canonical Allele Identifier: CA2650261391
Gene: CR2 HGNC NCBI

Linked Data

gnomAD v4: 1-207454382-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454383del , CM000663.2:g.207454383del GRCh38
NC_000001.10:g.207627728del , CM000663.1:g.207627728del GRCh37
NC_000001.9:g.205694351del NCBI36
NG_013006.1:g.5084del , LRG_348:g.5084del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699620.1:c.-478del ENSP00000514480.1:n.-478del
ENST00000699640.1:c.-385+1288del ENSP00000514493.1:n.-385+1288del
ENST00000367057.8:c.-36del MANE Select ENSP00000356024.3:n.-36del
ENST00000367057.7:c.-36del ENSP00000356024.3:n.-36del
ENST00000367058.7:c.-36del ENSP00000356025.3:n.-36del
ENST00000367059.3:c.-36del ENSP00000356026.3:n.-36del
NM_001006658.2:c.-36del , LRG_348t1:c.-36del NP_001006659.1:n.-36del
NM_001877.4:c.-36del NP_001868.2:n.-36del
NM_001006658.3:c.-36del MANE Select NP_001006659.1:n.-36del
NM_001877.5:c.-36del NP_001868.2:n.-36del
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