Canonical Allele Identifier: CA1268336299

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859821_88859834delinsACTCTTTAAAATAT , CM000664.2:g.88859821_88859834delinsACTCTTTAAAATAT GRCh38
NC_000002.11:g.89159333_89159346delinsACTCTTTAAAATAT , CM000664.1:g.89159333_89159346delinsACTCTTTAAAATAT GRCh37
NC_000002.10:g.88940448_88940461delinsACTCTTTAAAATAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2052_388+2065delinsATATTTTAAAGAGT (IGKV1-12) ENSP00000480537.2:n.388+2052_388+2065delinsATATTTTAAAGAGT
ENST00000430694.5:c.37+1052_37+1065delinsATATTTTAAAGAGT (IGKC) ENSP00000481923.2:n.37+1052_37+1065delinsATATTTTAAAGAGT
ENST00000610638.3:c.397+1691_397+1704delinsATATTTTAAAGAGT (IGKC) ENSP00000484499.3:n.397+1691_397+1704delinsATATTTTAAAGAGT
ENST00000634828.1:c.382+1691_382+1704delinsATATTTTAAAGAGT (IGKV1-8) ENSP00000489500.1:n.382+1691_382+1704delinsATATTTTAAAGAGT