Canonical Allele Identifier: CA1268335958

Linked Data

dbSNP Id: rs1675114577

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859572_88859602del , CM000664.2:g.88859572_88859602del GRCh38
NC_000002.11:g.89159084_89159114del , CM000664.1:g.89159084_89159114del GRCh37
NC_000002.10:g.88940199_88940229del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1919_389-1889del (IGKV1-12) ENSP00000480537.2:n.389-1919_389-1889del
ENST00000430694.5:c.37+1284_37+1314del (IGKC) ENSP00000481923.2:n.37+1284_37+1314del
ENST00000610638.3:c.398-1919_398-1889del (IGKC) ENSP00000484499.3:n.398-1919_398-1889del
ENST00000634828.1:c.383-1919_383-1889del (IGKV1-8) ENSP00000489500.1:n.383-1919_383-1889del