Canonical Allele Identifier: CA460019968
Gene: NEFL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.24810174T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24952661T>A , CM000670.2:g.24952661T>A GRCh38
NC_000008.10:g.24810174T>A , CM000670.1:g.24810174T>A GRCh37
NC_000008.9:g.24866091T>A NCBI36
NG_008492.1:g.8957A>T , LRG_259:g.8957A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000610854.2:c.*149A>T MANE Select ENSP00000482169.2:n.*149A>T
ENST00000610854.1:c.*149A>T ENSP00000482169.1:n.*149A>T
ENST00000619417.1:c.*646A>T ENSP00000483690.1:n.*646A>T
NM_006158.4:c.*149A>T , LRG_259t1:c.*149A>T NP_006149.2:n.*149A>T
NM_006158.5:c.*149A>T MANE Select NP_006149.2:n.*149A>T
Search 100 bp 5'
Search 100 bp 3'