Canonical Allele Identifier: CA1268335914

Linked Data

dbSNP Id: rs1675111672

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859543_88859559del , CM000664.2:g.88859543_88859559del GRCh38
NC_000002.11:g.89159055_89159071del , CM000664.1:g.89159055_89159071del GRCh37
NC_000002.10:g.88940170_88940186del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1876_389-1860del (IGKV1-12) ENSP00000480537.2:n.389-1876_389-1860del
ENST00000430694.5:c.37+1327_37+1343del (IGKC) ENSP00000481923.2:n.37+1327_37+1343del
ENST00000610638.3:c.398-1876_398-1860del (IGKC) ENSP00000484499.3:n.398-1876_398-1860del
ENST00000634828.1:c.383-1876_383-1860del (IGKV1-8) ENSP00000489500.1:n.383-1876_383-1860del