Canonical Allele Identifier: CA460021211
Gene: NEFL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.24814122T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956608T>G , CM000670.2:g.24956608T>G GRCh38
NC_000008.10:g.24814122T>G , CM000670.1:g.24814122T>G GRCh37
NC_000008.9:g.24870039T>G NCBI36
NG_008492.1:g.5010A>C , LRG_259:g.5010A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.-93A>C MANE Select ENSP00000482169.2:n.-93A>C
ENST00000610854.1:c.-93A>C ENSP00000482169.1:n.-93A>C
ENST00000615973.1:n.114A>C
ENST00000619417.1:c.-93A>C ENSP00000483690.1:n.-93A>C
NM_006158.4:c.-93A>C , LRG_259t1:c.-93A>C NP_006149.2:n.-93A>C
NM_006158.5:c.-93A>C MANE Select NP_006149.2:n.-93A>C
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