Canonical Allele Identifier: CA1771622541
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956808G= , CM000670.2:g.24956808G= GRCh38
NC_000008.10:g.24814322G= , CM000670.1:g.24814322G= GRCh37
NC_000008.9:g.24870239G= NCBI36
NG_008492.1:g.4810C= , LRG_259:g.4810C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-293C= ENSP00000482169.1:n.-293C=
NM_006158.4:c.-293C= , LRG_259t1:c.-293C= NP_006149.2:n.-293C=