Canonical Allele Identifier: CA2601816957

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859657_88859660del , CM000664.2:g.88859657_88859660del GRCh38
NC_000002.11:g.89159169_89159172del , CM000664.1:g.89159169_89159172del GRCh37
NC_000002.10:g.88940284_88940287del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1977_389-1974del (IGKV1-12) ENSP00000480537.2:n.389-1977_389-1974del
ENST00000430694.5:c.37+1226_37+1229del (IGKC) ENSP00000481923.2:n.37+1226_37+1229del
ENST00000610638.3:c.397+1865_397+1868del (IGKC) ENSP00000484499.3:n.397+1865_397+1868del
ENST00000634828.1:c.382+1865_382+1868del (IGKV1-8) ENSP00000489500.1:n.382+1865_382+1868del