Canonical Allele Identifier: CA1268336279

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859807_88859808delinsTA , CM000664.2:g.88859807_88859808delinsTA GRCh38
NC_000002.11:g.89159319_89159320delinsTA , CM000664.1:g.89159319_89159320delinsTA GRCh37
NC_000002.10:g.88940434_88940435delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2078_388+2079delinsTA (IGKV1-12) ENSP00000480537.2:n.388+2078_388+2079delinsTA
ENST00000430694.5:c.37+1078_37+1079delinsTA (IGKC) ENSP00000481923.2:n.37+1078_37+1079delinsTA
ENST00000610638.3:c.397+1717_397+1718delinsTA (IGKC) ENSP00000484499.3:n.397+1717_397+1718delinsTA
ENST00000634828.1:c.382+1717_382+1718delinsTA (IGKV1-8) ENSP00000489500.1:n.382+1717_382+1718delinsTA