Canonical Allele Identifier: CA1771622215
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956676_24956678delinsGAT , CM000670.2:g.24956676_24956678delinsGAT GRCh38
NC_000008.10:g.24814190_24814192delinsGAT , CM000670.1:g.24814190_24814192delinsGAT GRCh37
NC_000008.9:g.24870107_24870109delinsGAT NCBI36
NG_008492.1:g.4940_4942delinsATC , LRG_259:g.4940_4942delinsATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-163_-161delinsATC ENSP00000482169.1:n.-163_-161delinsATC
ENST00000615973.1:n.44_46delinsATC
NM_006158.4:c.-163_-161delinsATC , LRG_259t1:c.-163_-161delinsATC NP_006149.2:n.-163_-161delinsATC