Canonical Allele Identifier: CA370622277
Gene: NEFL HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956029C>T , CM000670.2:g.24956029C>T GRCh38
NC_000008.10:g.24813543C>T , CM000670.1:g.24813543C>T GRCh37
NC_000008.9:g.24869460C>T NCBI36
NG_008492.1:g.5589G>A , LRG_259:g.5589G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.487G>A MANE Select ENSP00000482169.2:p.Glu163Lys
ENST00000610854.1:c.487G>A ENSP00000482169.1:p.Glu163Lys
ENST00000615973.1:n.693G>A
ENST00000619417.1:c.487G>A ENSP00000483690.1:p.Glu163Lys
NM_006158.4:c.487G>A , LRG_259t1:c.487G>A NP_006149.2:p.Glu163Lys
NM_006158.5:c.487G>A MANE Select NP_006149.2:p.Glu163Lys