Canonical Allele Identifier: CA2601816986

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859692_88859693insTCT , CM000664.2:g.88859692_88859693insTCT GRCh38
NC_000002.11:g.89159204_89159205insTCT , CM000664.1:g.89159204_89159205insTCT GRCh37
NC_000002.10:g.88940319_88940320insTCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-2010_389-2009insAGA (IGKV1-12) ENSP00000480537.2:n.389-2010_389-2009insAGA
ENST00000430694.5:c.37+1193_37+1194insAGA (IGKC) ENSP00000481923.2:n.37+1193_37+1194insAGA
ENST00000610638.3:c.397+1832_397+1833insAGA (IGKC) ENSP00000484499.3:n.397+1832_397+1833insAGA
ENST00000634828.1:c.382+1832_382+1833insAGA (IGKV1-8) ENSP00000489500.1:n.382+1832_382+1833insAGA