Canonical Allele Identifier: CA1268335920

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859545_88859546delinsAG , CM000664.2:g.88859545_88859546delinsAG GRCh38
NC_000002.11:g.89159057_89159058delinsAG , CM000664.1:g.89159057_89159058delinsAG GRCh37
NC_000002.10:g.88940172_88940173delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1863_389-1862delinsCT (IGKV1-12) ENSP00000480537.2:n.389-1863_389-1862delinsCT
ENST00000430694.5:c.37+1340_37+1341delinsCT (IGKC) ENSP00000481923.2:n.37+1340_37+1341delinsCT
ENST00000610638.3:c.398-1863_398-1862delinsCT (IGKC) ENSP00000484499.3:n.398-1863_398-1862delinsCT
ENST00000634828.1:c.383-1863_383-1862delinsCT (IGKV1-8) ENSP00000489500.1:n.383-1863_383-1862delinsCT