Canonical Allele Identifier: CA1771622141
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956628T= , CM000670.2:g.24956628T= GRCh38
NC_000008.10:g.24814142T= , CM000670.1:g.24814142T= GRCh37
NC_000008.9:g.24870059T= NCBI36
NG_008492.1:g.4990A= , LRG_259:g.4990A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-113A= ENSP00000482169.1:n.-113A=
ENST00000615973.1:n.94A=
NM_006158.4:c.-113A= , LRG_259t1:c.-113A= NP_006149.2:n.-113A=