Canonical Allele Identifier: CA1268336272

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859804_88859806delinsGGA , CM000664.2:g.88859804_88859806delinsGGA GRCh38
NC_000002.11:g.89159316_89159318delinsGGA , CM000664.1:g.89159316_89159318delinsGGA GRCh37
NC_000002.10:g.88940431_88940433delinsGGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2080_388+2082delinsTCC (IGKV1-12) ENSP00000480537.2:n.388+2080_388+2082delinsTCC
ENST00000430694.5:c.37+1080_37+1082delinsTCC (IGKC) ENSP00000481923.2:n.37+1080_37+1082delinsTCC
ENST00000610638.3:c.397+1719_397+1721delinsTCC (IGKC) ENSP00000484499.3:n.397+1719_397+1721delinsTCC
ENST00000634828.1:c.382+1719_382+1721delinsTCC (IGKV1-8) ENSP00000489500.1:n.382+1719_382+1721delinsTCC