Canonical Allele Identifier: CA1268335986

Linked Data

dbSNP Id: rs1675116101

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859591_88859604del , CM000664.2:g.88859591_88859604del GRCh38
NC_000002.11:g.89159103_89159116del , CM000664.1:g.89159103_89159116del GRCh37
NC_000002.10:g.88940218_88940231del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1920_389-1907del (IGKV1-12) ENSP00000480537.2:n.389-1920_389-1907del
ENST00000430694.5:c.37+1283_37+1296del (IGKC) ENSP00000481923.2:n.37+1283_37+1296del
ENST00000610638.3:c.398-1920_398-1907del (IGKC) ENSP00000484499.3:n.398-1920_398-1907del
ENST00000634828.1:c.383-1920_383-1907del (IGKV1-8) ENSP00000489500.1:n.383-1920_383-1907del