Canonical Allele Identifier: CA1771650809
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24952562C= , CM000670.2:g.24952562C= GRCh38
NC_000008.10:g.24810075C= , CM000670.1:g.24810075C= GRCh37
NC_000008.9:g.24865992C= NCBI36
NG_008492.1:g.9056G= , LRG_259:g.9056G=

Transcript Alleles

HGVS Amino-acid change
ENST00000610854.2:c.*248G= MANE Select ENSP00000482169.2:n.*248G=
ENST00000610854.1:c.*248G= ENSP00000482169.1:n.*248G=
ENST00000619417.1:c.*745G= ENSP00000483690.1:n.*745G=
NM_006158.4:c.*248G= , LRG_259t1:c.*248G= NP_006149.2:n.*248G=
NM_006158.5:c.*248G= MANE Select NP_006149.2:n.*248G=