Canonical Allele Identifier: CA2601816921

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859627_88859630del , CM000664.2:g.88859627_88859630del GRCh38
NC_000002.11:g.89159139_89159142del , CM000664.1:g.89159139_89159142del GRCh37
NC_000002.10:g.88940254_88940257del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1947_389-1944del (IGKV1-12) ENSP00000480537.2:n.389-1947_389-1944del
ENST00000430694.5:c.37+1256_37+1259del (IGKC) ENSP00000481923.2:n.37+1256_37+1259del
ENST00000610638.3:c.397+1895_397+1898del (IGKC) ENSP00000484499.3:n.397+1895_397+1898del
ENST00000634828.1:c.382+1895_382+1898del (IGKV1-8) ENSP00000489500.1:n.382+1895_382+1898del