Canonical Allele Identifier: CA646854733

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859742_88859752del , CM000664.2:g.88859742_88859752del GRCh38
NC_000002.11:g.89159254_89159264del , CM000664.1:g.89159254_89159264del GRCh37
NC_000002.10:g.88940369_88940379del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2068_389-2058del (IGKV1-12) ENSP00000480537.2:n.389-2068_389-2058del
ENST00000430694.5:c.37+1135_37+1145del (IGKC) ENSP00000481923.2:n.37+1135_37+1145del
ENST00000610638.3:c.397+1774_397+1784del (IGKC) ENSP00000484499.3:n.397+1774_397+1784del
ENST00000634828.1:c.382+1774_382+1784del (IGKV1-8) ENSP00000489500.1:n.382+1774_382+1784del