Canonical Allele Identifier: CA2601816880

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859605_88859606insT , CM000664.2:g.88859605_88859606insT GRCh38
NC_000002.11:g.89159117_89159118insT , CM000664.1:g.89159117_89159118insT GRCh37
NC_000002.10:g.88940232_88940233insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.389-1923_389-1922insA (IGKV1-12) ENSP00000480537.2:n.389-1923_389-1922insA
ENST00000430694.5:c.37+1280_37+1281insA (IGKC) ENSP00000481923.2:n.37+1280_37+1281insA
ENST00000610638.3:c.397+1919_397+1920insA (IGKC) ENSP00000484499.3:n.397+1919_397+1920insA
ENST00000634828.1:c.382+1919_382+1920insA (IGKV1-8) ENSP00000489500.1:n.382+1919_382+1920insA