Canonical Allele Identifier: CA2750862388

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859361_88859364del , CM000664.2:g.88859361_88859364del GRCh38
NC_000002.11:g.89158874_89158877del , CM000664.1:g.89158874_89158877del GRCh37
NC_000002.10:g.88939989_88939992del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377423.6:c.389-1681_389-1678del (IGKV1-12) ENSP00000480537.2:n.389-1681_389-1678del
ENST00000430694.5:c.37+1522_37+1525del (IGKC) ENSP00000481923.2:n.37+1522_37+1525del
ENST00000610638.3:c.398-1681_398-1678del (IGKC) ENSP00000484499.3:n.398-1681_398-1678del
ENST00000634828.1:c.383-1681_383-1678del (IGKV1-8) ENSP00000489500.1:n.383-1681_383-1678del