Canonical Allele Identifier: CA1268336013

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859606_88859608delinsCAT , CM000664.2:g.88859606_88859608delinsCAT GRCh38
NC_000002.11:g.89159118_89159120delinsCAT , CM000664.1:g.89159118_89159120delinsCAT GRCh37
NC_000002.10:g.88940233_88940235delinsCAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1925_389-1923delinsATG (IGKV1-12) ENSP00000480537.2:n.389-1925_389-1923delinsATG
ENST00000430694.5:c.37+1278_37+1280delinsATG (IGKC) ENSP00000481923.2:n.37+1278_37+1280delinsATG
ENST00000610638.3:c.397+1917_397+1919delinsATG (IGKC) ENSP00000484499.3:n.397+1917_397+1919delinsATG
ENST00000634828.1:c.382+1917_382+1919delinsATG (IGKV1-8) ENSP00000489500.1:n.382+1917_382+1919delinsATG