Canonical Allele Identifier: CA460021209

Gene: NEFL

Linked Data

• MyVariant Identifiers: chr8:g.24814122T>A (hg19)

Genomic Alleles

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

Transcript Alleles

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