Canonical Allele Identifier: CA2716802238
Gene: NEFL HGNC NCBI

Linked Data

dbSNP Id: rs2117256516

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956782del , CM000670.2:g.24956782del GRCh38
NC_000008.10:g.24814296del , CM000670.1:g.24814296del GRCh37
NC_000008.9:g.24870213del NCBI36
NG_008492.1:g.4837del , LRG_259:g.4837del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-266del ENSP00000482169.1:n.-266del
NM_006158.4:c.-266del , LRG_259t1:c.-266del NP_006149.2:n.-266del