Canonical Allele Identifier: CA1268336285

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859811_88859812delinsGA , CM000664.2:g.88859811_88859812delinsGA GRCh38
NC_000002.11:g.89159323_89159324delinsGA , CM000664.1:g.89159323_89159324delinsGA GRCh37
NC_000002.10:g.88940438_88940439delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2074_388+2075delinsTC (IGKV1-12) ENSP00000480537.2:n.388+2074_388+2075delinsTC
ENST00000430694.5:c.37+1074_37+1075delinsTC (IGKC) ENSP00000481923.2:n.37+1074_37+1075delinsTC
ENST00000610638.3:c.397+1713_397+1714delinsTC (IGKC) ENSP00000484499.3:n.397+1713_397+1714delinsTC
ENST00000634828.1:c.382+1713_382+1714delinsTC (IGKV1-8) ENSP00000489500.1:n.382+1713_382+1714delinsTC