Canonical Allele Identifier: CA1771622387
Gene: NEFL HGNC NCBI

Linked Data

dbSNP Id: rs1803064559

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956744del , CM000670.2:g.24956744del GRCh38
NC_000008.10:g.24814258del , CM000670.1:g.24814258del GRCh37
NC_000008.9:g.24870175del NCBI36
NG_008492.1:g.4876del , LRG_259:g.4876del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-227del ENSP00000482169.1:n.-227del
NM_006158.4:c.-227del , LRG_259t1:c.-227del NP_006149.2:n.-227del