Canonical Allele Identifier: CA646854943

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859819dup , CM000664.2:g.88859819dup GRCh38
NC_000002.11:g.89159331dup , CM000664.1:g.89159331dup GRCh37
NC_000002.10:g.88940446dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2067dup (IGKV1-12) ENSP00000480537.2:n.388+2067dup
ENST00000430694.5:c.37+1067dup (IGKC) ENSP00000481923.2:n.37+1067dup
ENST00000610638.3:c.397+1706dup (IGKC) ENSP00000484499.3:n.397+1706dup
ENST00000634828.1:c.382+1706dup (IGKV1-8) ENSP00000489500.1:n.382+1706dup