Canonical Allele Identifier: CA1268336283

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859810_88859811delinsTG , CM000664.2:g.88859810_88859811delinsTG GRCh38
NC_000002.11:g.89159322_89159323delinsTG , CM000664.1:g.89159322_89159323delinsTG GRCh37
NC_000002.10:g.88940437_88940438delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2075_388+2076delinsCA (IGKV1-12) ENSP00000480537.2:n.388+2075_388+2076delinsCA
ENST00000430694.5:c.37+1075_37+1076delinsCA (IGKC) ENSP00000481923.2:n.37+1075_37+1076delinsCA
ENST00000610638.3:c.397+1714_397+1715delinsCA (IGKC) ENSP00000484499.3:n.397+1714_397+1715delinsCA
ENST00000634828.1:c.382+1714_382+1715delinsCA (IGKV1-8) ENSP00000489500.1:n.382+1714_382+1715delinsCA