Canonical Allele Identifier: CA1771622138
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956627C= , CM000670.2:g.24956627C= GRCh38
NC_000008.10:g.24814141C= , CM000670.1:g.24814141C= GRCh37
NC_000008.9:g.24870058C= NCBI36
NG_008492.1:g.4991G= , LRG_259:g.4991G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-112G= ENSP00000482169.1:n.-112G=
ENST00000615973.1:n.95G=
NM_006158.4:c.-112G= , LRG_259t1:c.-112G= NP_006149.2:n.-112G=