Canonical Allele Identifier: CA1771622239
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956680A= , CM000670.2:g.24956680A= GRCh38
NC_000008.10:g.24814194A= , CM000670.1:g.24814194A= GRCh37
NC_000008.9:g.24870111A= NCBI36
NG_008492.1:g.4938T= , LRG_259:g.4938T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-165T= ENSP00000482169.1:n.-165T=
ENST00000615973.1:n.42T=
NM_006158.4:c.-165T= , LRG_259t1:c.-165T= NP_006149.2:n.-165T=