Canonical Allele Identifier: CA1771622168
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956646G= , CM000670.2:g.24956646G= GRCh38
NC_000008.10:g.24814160G= , CM000670.1:g.24814160G= GRCh37
NC_000008.9:g.24870077G= NCBI36
NG_008492.1:g.4972C= , LRG_259:g.4972C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-131C= ENSP00000482169.1:n.-131C=
ENST00000615973.1:n.76C=
NM_006158.4:c.-131C= , LRG_259t1:c.-131C= NP_006149.2:n.-131C=