Canonical Allele Identifier: CA1268336039

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859623_88859624delinsAC , CM000664.2:g.88859623_88859624delinsAC GRCh38
NC_000002.11:g.89159135_89159136delinsAC , CM000664.1:g.89159135_89159136delinsAC GRCh37
NC_000002.10:g.88940250_88940251delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1941_389-1940delinsGT (IGKV1-12) ENSP00000480537.2:n.389-1941_389-1940delinsGT
ENST00000430694.5:c.37+1262_37+1263delinsGT (IGKC) ENSP00000481923.2:n.37+1262_37+1263delinsGT
ENST00000610638.3:c.397+1901_397+1902delinsGT (IGKC) ENSP00000484499.3:n.397+1901_397+1902delinsGT
ENST00000634828.1:c.382+1901_382+1902delinsGT (IGKV1-8) ENSP00000489500.1:n.382+1901_382+1902delinsGT