Canonical Allele Identifier: CA1268336096

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859674_88859680delinsGGCGGCT , CM000664.2:g.88859674_88859680delinsGGCGGCT GRCh38
NC_000002.11:g.89159186_89159192delinsGGCGGCT , CM000664.1:g.89159186_89159192delinsGGCGGCT GRCh37
NC_000002.10:g.88940301_88940307delinsGGCGGCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1997_389-1991delinsAGCCGCC (IGKV1-12) ENSP00000480537.2:n.389-1997_389-1991delinsAGCCGCC
ENST00000430694.5:c.37+1206_37+1212delinsAGCCGCC (IGKC) ENSP00000481923.2:n.37+1206_37+1212delinsAGCCGCC
ENST00000610638.3:c.397+1845_397+1851delinsAGCCGCC (IGKC) ENSP00000484499.3:n.397+1845_397+1851delinsAGCCGCC
ENST00000634828.1:c.382+1845_382+1851delinsAGCCGCC (IGKV1-8) ENSP00000489500.1:n.382+1845_382+1851delinsAGCCGCC