Canonical Allele Identifier: CA1033367067

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859754_88859755insT , CM000664.2:g.88859754_88859755insT GRCh38
NC_000002.11:g.89159266_89159267insT , CM000664.1:g.89159266_89159267insT GRCh37
NC_000002.10:g.88940381_88940382insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2072_389-2071insA (IGKV1-12) ENSP00000480537.2:n.389-2072_389-2071insA
ENST00000430694.5:c.37+1131_37+1132insA (IGKC) ENSP00000481923.2:n.37+1131_37+1132insA
ENST00000610638.3:c.397+1770_397+1771insA (IGKC) ENSP00000484499.3:n.397+1770_397+1771insA
ENST00000634828.1:c.382+1770_382+1771insA (IGKV1-8) ENSP00000489500.1:n.382+1770_382+1771insA