Canonical Allele Identifier: CA1771622116
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956618G= , CM000670.2:g.24956618G= GRCh38
NC_000008.10:g.24814132G= , CM000670.1:g.24814132G= GRCh37
NC_000008.9:g.24870049G= NCBI36
NG_008492.1:g.5000C= , LRG_259:g.5000C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-103C= ENSP00000482169.1:n.-103C=
ENST00000615973.1:n.104C=
NM_006158.4:c.-103C= , LRG_259t1:c.-103C= NP_006149.2:n.-103C=