Canonical Allele Identifier: CA1033366873

Linked Data

dbSNP Id: rs1675123401

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859677_88859682del , CM000664.2:g.88859677_88859682del GRCh38
NC_000002.11:g.89159189_89159194del , CM000664.1:g.89159189_89159194del GRCh37
NC_000002.10:g.88940304_88940309del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1997_389-1992del (IGKV1-12) ENSP00000480537.2:n.389-1997_389-1992del
ENST00000430694.5:c.37+1206_37+1211del (IGKC) ENSP00000481923.2:n.37+1206_37+1211del
ENST00000610638.3:c.397+1845_397+1850del (IGKC) ENSP00000484499.3:n.397+1845_397+1850del
ENST00000634828.1:c.382+1845_382+1850del (IGKV1-8) ENSP00000489500.1:n.382+1845_382+1850del