Canonical Allele Identifier: CA1771622135
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956626T= , CM000670.2:g.24956626T= GRCh38
NC_000008.10:g.24814140T= , CM000670.1:g.24814140T= GRCh37
NC_000008.9:g.24870057T= NCBI36
NG_008492.1:g.4992A= , LRG_259:g.4992A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-111A= ENSP00000482169.1:n.-111A=
ENST00000615973.1:n.96A=
NM_006158.4:c.-111A= , LRG_259t1:c.-111A= NP_006149.2:n.-111A=