Canonical Allele Identifier: CA2601816499

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859353_88859362del , CM000664.2:g.88859353_88859362del GRCh38
NC_000002.11:g.89158866_89158875del , CM000664.1:g.89158866_89158875del GRCh37
NC_000002.10:g.88939981_88939990del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377423.6:c.389-1679_389-1670del (IGKV1-12) ENSP00000480537.2:n.389-1679_389-1670del
ENST00000430694.5:c.37+1524_37+1533del (IGKC) ENSP00000481923.2:n.37+1524_37+1533del
ENST00000610638.3:c.398-1679_398-1670del (IGKC) ENSP00000484499.3:n.398-1679_398-1670del
ENST00000634828.1:c.383-1679_383-1670del (IGKV1-8) ENSP00000489500.1:n.383-1679_383-1670del