Canonical Allele Identifier: CA460019676
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24952559-G-A
MyVariant Identifiers: chr8:g.24810072G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24952559G>A , CM000670.2:g.24952559G>A GRCh38
NC_000008.10:g.24810072G>A , CM000670.1:g.24810072G>A GRCh37
NC_000008.9:g.24865989G>A NCBI36
NG_008492.1:g.9059C>T , LRG_259:g.9059C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.*251C>T MANE Select ENSP00000482169.2:n.*251C>T
ENST00000610854.1:c.*251C>T ENSP00000482169.1:n.*251C>T
ENST00000619417.1:c.*748C>T ENSP00000483690.1:n.*748C>T
NM_006158.4:c.*251C>T , LRG_259t1:c.*251C>T NP_006149.2:n.*251C>T
NM_006158.5:c.*251C>T MANE Select NP_006149.2:n.*251C>T