Canonical Allele Identifier: CA2601816912

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859621_88859622del , CM000664.2:g.88859621_88859622del GRCh38
NC_000002.11:g.89159133_89159134del , CM000664.1:g.89159133_89159134del GRCh37
NC_000002.10:g.88940248_88940249del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1939_389-1938del (IGKV1-12) ENSP00000480537.2:n.389-1939_389-1938del
ENST00000430694.5:c.37+1264_37+1265del (IGKC) ENSP00000481923.2:n.37+1264_37+1265del
ENST00000610638.3:c.397+1903_397+1904del (IGKC) ENSP00000484499.3:n.397+1903_397+1904del
ENST00000634828.1:c.382+1903_382+1904del (IGKV1-8) ENSP00000489500.1:n.382+1903_382+1904del