Canonical Allele Identifier: CA2601816909

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859617_88859618del , CM000664.2:g.88859617_88859618del GRCh38
NC_000002.11:g.89159129_89159130del , CM000664.1:g.89159129_89159130del GRCh37
NC_000002.10:g.88940244_88940245del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1935_389-1934del (IGKV1-12) ENSP00000480537.2:n.389-1935_389-1934del
ENST00000430694.5:c.37+1268_37+1269del (IGKC) ENSP00000481923.2:n.37+1268_37+1269del
ENST00000610638.3:c.397+1907_397+1908del (IGKC) ENSP00000484499.3:n.397+1907_397+1908del
ENST00000634828.1:c.382+1907_382+1908del (IGKV1-8) ENSP00000489500.1:n.382+1907_382+1908del