Canonical Allele Identifier: CA2601816888

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859608_88859613del , CM000664.2:g.88859608_88859613del GRCh38
NC_000002.11:g.89159120_89159125del , CM000664.1:g.89159120_89159125del GRCh37
NC_000002.10:g.88940235_88940240del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1929_389-1924del (IGKV1-12) ENSP00000480537.2:n.389-1929_389-1924del
ENST00000430694.5:c.37+1274_37+1279del (IGKC) ENSP00000481923.2:n.37+1274_37+1279del
ENST00000610638.3:c.397+1913_397+1918del (IGKC) ENSP00000484499.3:n.397+1913_397+1918del
ENST00000634828.1:c.382+1913_382+1918del (IGKV1-8) ENSP00000489500.1:n.382+1913_382+1918del