Canonical Allele Identifier: CA646854959

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859822_88859824del , CM000664.2:g.88859822_88859824del GRCh38
NC_000002.11:g.89159334_89159336del , CM000664.1:g.89159334_89159336del GRCh37
NC_000002.10:g.88940449_88940451del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377423.6:c.388+2062_388+2064del (IGKV1-12) ENSP00000480537.2:n.388+2062_388+2064del
ENST00000430694.5:c.37+1062_37+1064del (IGKC) ENSP00000481923.2:n.37+1062_37+1064del
ENST00000610638.3:c.397+1701_397+1703del (IGKC) ENSP00000484499.3:n.397+1701_397+1703del
ENST00000634828.1:c.382+1701_382+1703del (IGKV1-8) ENSP00000489500.1:n.382+1701_382+1703del