Canonical Allele Identifier: CA1771622482
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956772_24956778delinsAGCTGCG , CM000670.2:g.24956772_24956778delinsAGCTGCG GRCh38
NC_000008.10:g.24814286_24814292delinsAGCTGCG , CM000670.1:g.24814286_24814292delinsAGCTGCG GRCh37
NC_000008.9:g.24870203_24870209delinsAGCTGCG NCBI36
NG_008492.1:g.4840_4846delinsCGCAGCT , LRG_259:g.4840_4846delinsCGCAGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-263_-257delinsCGCAGCT ENSP00000482169.1:n.-263_-257delinsCGCAGCT
NM_006158.4:c.-263_-257delinsCGCAGCT , LRG_259t1:c.-263_-257delinsCGCAGCT NP_006149.2:n.-263_-257delinsCGCAGCT