Canonical Allele Identifier: CA1771650640
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24952443C= , CM000670.2:g.24952443C= GRCh38
NC_000008.10:g.24809956C= , CM000670.1:g.24809956C= GRCh37
NC_000008.9:g.24865873C= NCBI36
NG_008492.1:g.9175G= , LRG_259:g.9175G=

Transcript Alleles

HGVS Amino-acid change
ENST00000610854.2:c.*367G= MANE Select ENSP00000482169.2:n.*367G=
ENST00000610854.1:c.*367G= ENSP00000482169.1:n.*367G=
ENST00000619417.1:c.*864G= ENSP00000483690.1:n.*864G=
NM_006158.4:c.*367G= , LRG_259t1:c.*367G= NP_006149.2:n.*367G=
NM_006158.5:c.*367G= MANE Select NP_006149.2:n.*367G=