Canonical Allele Identifier: CA370624198
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956467-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956467G>A , CM000670.2:g.24956467G>A GRCh38
NC_000008.10:g.24813981G>A , CM000670.1:g.24813981G>A GRCh37
NC_000008.9:g.24869898G>A NCBI36
NG_008492.1:g.5151C>T , LRG_259:g.5151C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.49C>T MANE Select ENSP00000482169.2:p.Arg17Cys
ENST00000610854.1:c.49C>T ENSP00000482169.1:p.Arg17Cys
ENST00000615973.1:n.255C>T
ENST00000619417.1:c.49C>T ENSP00000483690.1:p.Arg17Cys
NM_006158.4:c.49C>T , LRG_259t1:c.49C>T NP_006149.2:p.Arg17Cys
NM_006158.5:c.49C>T MANE Select NP_006149.2:p.Arg17Cys