Canonical Allele Identifier: CA1771622195
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956661A= , CM000670.2:g.24956661A= GRCh38
NC_000008.10:g.24814175A= , CM000670.1:g.24814175A= GRCh37
NC_000008.9:g.24870092A= NCBI36
NG_008492.1:g.4957T= , LRG_259:g.4957T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-146T= ENSP00000482169.1:n.-146T=
ENST00000615973.1:n.61T=
NM_006158.4:c.-146T= , LRG_259t1:c.-146T= NP_006149.2:n.-146T=