Canonical Allele Identifier: CA51502551

Linked Data

dbSNP Id: rs796955349

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859763_88859765delinsACT , CM000664.2:g.88859763_88859765delinsACT GRCh38
NC_000002.11:g.89159275_89159277delinsACT , CM000664.1:g.89159275_89159277delinsACT GRCh37
NC_000002.10:g.88940390_88940392delinsACT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2082_389-2080delinsAGT (IGKV1-12) ENSP00000480537.2:n.389-2082_389-2080delinsAGT
ENST00000430694.5:c.37+1121_37+1123delinsAGT (IGKC) ENSP00000481923.2:n.37+1121_37+1123delinsAGT
ENST00000610638.3:c.397+1760_397+1762delinsAGT (IGKC) ENSP00000484499.3:n.397+1760_397+1762delinsAGT
ENST00000634828.1:c.382+1760_382+1762delinsAGT (IGKV1-8) ENSP00000489500.1:n.382+1760_382+1762delinsAGT