Canonical Allele Identifier: CA1771621825
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956516G= , CM000670.2:g.24956516G= GRCh38
NC_000008.10:g.24814030G= , CM000670.1:g.24814030G= GRCh37
NC_000008.9:g.24869947G= NCBI36
NG_008492.1:g.5102C= , LRG_259:g.5102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.-1C= MANE Select ENSP00000482169.2:n.-1C=
ENST00000610854.1:c.-1C= ENSP00000482169.1:n.-1C=
ENST00000615973.1:n.206C=
ENST00000619417.1:c.-1C= ENSP00000483690.1:n.-1C=
NM_006158.4:c.-1C= , LRG_259t1:c.-1C= NP_006149.2:n.-1C=
NM_006158.5:c.-1C= MANE Select NP_006149.2:n.-1C=