Canonical Allele Identifier: CA1771621640
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956457T= , CM000670.2:g.24956457T= GRCh38
NC_000008.10:g.24813971T= , CM000670.1:g.24813971T= GRCh37
NC_000008.9:g.24869888T= NCBI36
NG_008492.1:g.5161A= , LRG_259:g.5161A=

Transcript Alleles

HGVS Amino-acid change
ENST00000610854.2:c.59A= MANE Select ENSP00000482169.2:p.Glu20=
ENST00000610854.1:c.59A= ENSP00000482169.1:p.Glu20=
ENST00000615973.1:n.265A=
ENST00000619417.1:c.59A= ENSP00000483690.1:p.Glu20=
NM_006158.4:c.59A= , LRG_259t1:c.59A= NP_006149.2:p.Glu20=
NM_006158.5:c.59A= MANE Select NP_006149.2:p.Glu20=