Canonical Allele Identifier: CA1771622189
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956660G= , CM000670.2:g.24956660G= GRCh38
NC_000008.10:g.24814174G= , CM000670.1:g.24814174G= GRCh37
NC_000008.9:g.24870091G= NCBI36
NG_008492.1:g.4958C= , LRG_259:g.4958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-145C= ENSP00000482169.1:n.-145C=
ENST00000615973.1:n.62C=
NM_006158.4:c.-145C= , LRG_259t1:c.-145C= NP_006149.2:n.-145C=