Canonical Allele Identifier: CA2601816929

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859628_88859629del , CM000664.2:g.88859628_88859629del GRCh38
NC_000002.11:g.89159140_89159141del , CM000664.1:g.89159140_89159141del GRCh37
NC_000002.10:g.88940255_88940256del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1946_389-1945del (IGKV1-12) ENSP00000480537.2:n.389-1946_389-1945del
ENST00000430694.5:c.37+1257_37+1258del (IGKC) ENSP00000481923.2:n.37+1257_37+1258del
ENST00000610638.3:c.397+1896_397+1897del (IGKC) ENSP00000484499.3:n.397+1896_397+1897del
ENST00000634828.1:c.382+1896_382+1897del (IGKV1-8) ENSP00000489500.1:n.382+1896_382+1897del