Canonical Allele Identifier: CA2617768277
Gene: PLBD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14506892dup , CM000674.2:g.14506892dup GRCh38
NC_000012.11:g.14659826dup , CM000674.1:g.14659826dup GRCh37
NC_000012.10:g.14551093dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000240617.10:c.1372+44dup MANE Select ENSP00000240617.5:n.1372+44dup
ENST00000240617.9:c.1372+44dup ENSP00000240617.5:n.1372+44dup
NM_024829.5:c.1372+44dup NP_079105.4:n.1372+44dup
NM_024829.6:c.1372+44dup MANE Select NP_079105.4:n.1372+44dup