Canonical Allele Identifier: CA1771622161
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956643T= , CM000670.2:g.24956643T= GRCh38
NC_000008.10:g.24814157T= , CM000670.1:g.24814157T= GRCh37
NC_000008.9:g.24870074T= NCBI36
NG_008492.1:g.4975A= , LRG_259:g.4975A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-128A= ENSP00000482169.1:n.-128A=
ENST00000615973.1:n.79A=
NM_006158.4:c.-128A= , LRG_259t1:c.-128A= NP_006149.2:n.-128A=