Canonical Allele Identifier: CA2601816972

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859674_88859684del , CM000664.2:g.88859674_88859684del GRCh38
NC_000002.11:g.89159186_89159196del , CM000664.1:g.89159186_89159196del GRCh37
NC_000002.10:g.88940301_88940311del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2001_389-1991del (IGKV1-12) ENSP00000480537.2:n.389-2001_389-1991del
ENST00000430694.5:c.37+1202_37+1212del (IGKC) ENSP00000481923.2:n.37+1202_37+1212del
ENST00000610638.3:c.397+1841_397+1851del (IGKC) ENSP00000484499.3:n.397+1841_397+1851del
ENST00000634828.1:c.382+1841_382+1851del (IGKV1-8) ENSP00000489500.1:n.382+1841_382+1851del