Canonical Allele Identifier: CA1771622384
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956741_24956742delinsAG , CM000670.2:g.24956741_24956742delinsAG GRCh38
NC_000008.10:g.24814255_24814256delinsAG , CM000670.1:g.24814255_24814256delinsAG GRCh37
NC_000008.9:g.24870172_24870173delinsAG NCBI36
NG_008492.1:g.4876_4877delinsCT , LRG_259:g.4876_4877delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-227_-226delinsCT ENSP00000482169.1:n.-227_-226delinsCT
NM_006158.4:c.-227_-226delinsCT , LRG_259t1:c.-227_-226delinsCT NP_006149.2:n.-227_-226delinsCT