Canonical Allele Identifier: CA1268336264

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859801_88859802delinsAG , CM000664.2:g.88859801_88859802delinsAG GRCh38
NC_000002.11:g.89159313_89159314delinsAG , CM000664.1:g.89159313_89159314delinsAG GRCh37
NC_000002.10:g.88940428_88940429delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2084_388+2085delinsCT (IGKV1-12) ENSP00000480537.2:n.388+2084_388+2085delinsCT
ENST00000430694.5:c.37+1084_37+1085delinsCT (IGKC) ENSP00000481923.2:n.37+1084_37+1085delinsCT
ENST00000610638.3:c.397+1723_397+1724delinsCT (IGKC) ENSP00000484499.3:n.397+1723_397+1724delinsCT
ENST00000634828.1:c.382+1723_382+1724delinsCT (IGKV1-8) ENSP00000489500.1:n.382+1723_382+1724delinsCT