Canonical Allele Identifier: CA2686596923
Gene: NEFL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956578dup , CM000670.2:g.24956578dup GRCh38
NC_000008.10:g.24814092dup , CM000670.1:g.24814092dup GRCh37
NC_000008.9:g.24870009dup NCBI36
NG_008492.1:g.5043dup , LRG_259:g.5043dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.-60dup MANE Select ENSP00000482169.2:n.-60dup
ENST00000610854.1:c.-60dup ENSP00000482169.1:n.-60dup
ENST00000615973.1:n.147dup
ENST00000619417.1:c.-60dup ENSP00000483690.1:n.-60dup
NM_006158.4:c.-60dup , LRG_259t1:c.-60dup NP_006149.2:n.-60dup
NM_006158.5:c.-60dup MANE Select NP_006149.2:n.-60dup