Canonical Allele Identifier: CA460019333
Gene: NEFL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.24809958A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24952445A>T , CM000670.2:g.24952445A>T GRCh38
NC_000008.10:g.24809958A>T , CM000670.1:g.24809958A>T GRCh37
NC_000008.9:g.24865875A>T NCBI36
NG_008492.1:g.9173T>A , LRG_259:g.9173T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.*365T>A MANE Select ENSP00000482169.2:n.*365T>A
ENST00000610854.1:c.*365T>A ENSP00000482169.1:n.*365T>A
ENST00000619417.1:c.*862T>A ENSP00000483690.1:n.*862T>A
NM_006158.4:c.*365T>A , LRG_259t1:c.*365T>A NP_006149.2:n.*365T>A
NM_006158.5:c.*365T>A MANE Select NP_006149.2:n.*365T>A
Search 100 bp 5'
Search 100 bp 3'