Canonical Allele Identifier: CA370624192
Gene: NEFL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956466C>A , CM000670.2:g.24956466C>A GRCh38
NC_000008.10:g.24813980C>A , CM000670.1:g.24813980C>A GRCh37
NC_000008.9:g.24869897C>A NCBI36
NG_008492.1:g.5152G>T , LRG_259:g.5152G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.50G>T MANE Select ENSP00000482169.2:p.Arg17Leu
ENST00000610854.1:c.50G>T ENSP00000482169.1:p.Arg17Leu
ENST00000615973.1:n.256G>T
ENST00000619417.1:c.50G>T ENSP00000483690.1:p.Arg17Leu
NM_006158.4:c.50G>T , LRG_259t1:c.50G>T NP_006149.2:p.Arg17Leu
NM_006158.5:c.50G>T MANE Select NP_006149.2:p.Arg17Leu