Canonical Allele Identifier: CA2686596932
Gene: NEFL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956701del , CM000670.2:g.24956701del GRCh38
NC_000008.10:g.24814215del , CM000670.1:g.24814215del GRCh37
NC_000008.9:g.24870132del NCBI36
NG_008492.1:g.4921del , LRG_259:g.4921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-182del ENSP00000482169.1:n.-182del
ENST00000615973.1:n.25del
NM_006158.4:c.-182del , LRG_259t1:c.-182del NP_006149.2:n.-182del