Canonical Allele Identifier: CA2601817078

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859768_88859775del , CM000664.2:g.88859768_88859775del GRCh38
NC_000002.11:g.89159280_89159287del , CM000664.1:g.89159280_89159287del GRCh37
NC_000002.10:g.88940395_88940402del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2092_389-2085del (IGKV1-12) ENSP00000480537.2:n.389-2092_389-2085del
ENST00000430694.5:c.37+1111_37+1118del (IGKC) ENSP00000481923.2:n.37+1111_37+1118del
ENST00000610638.3:c.397+1750_397+1757del (IGKC) ENSP00000484499.3:n.397+1750_397+1757del
ENST00000634828.1:c.382+1750_382+1757del (IGKV1-8) ENSP00000489500.1:n.382+1750_382+1757del