Canonical Allele Identifier: CA460020850
Gene: NEFL HGNC NCBI

Linked Data

ClinVar Variation Id: 2898300
ClinVar RCV Id: RCV003629651
MyVariant Identifiers: chr8:g.24813982C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956468C>G , CM000670.2:g.24956468C>G GRCh38
NC_000008.10:g.24813982C>G , CM000670.1:g.24813982C>G GRCh37
NC_000008.9:g.24869899C>G NCBI36
NG_008492.1:g.5150G>C , LRG_259:g.5150G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.48G>C MANE Select ENSP00000482169.2:p.Arg16=
ENST00000610854.1:c.48G>C ENSP00000482169.1:p.Arg16=
ENST00000615973.1:n.254G>C
ENST00000619417.1:c.48G>C ENSP00000483690.1:p.Arg16=
NM_006158.4:c.48G>C , LRG_259t1:c.48G>C NP_006149.2:p.Arg16=
NM_006158.5:c.48G>C MANE Select NP_006149.2:p.Arg16=