Canonical Allele Identifier: CA2686596939
Gene: NEFL HGNC NCBI

Linked Data

gnomAD v4: 8-24956791-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956793del , CM000670.2:g.24956793del GRCh38
NC_000008.10:g.24814307del , CM000670.1:g.24814307del GRCh37
NC_000008.9:g.24870224del NCBI36
NG_008492.1:g.4826del , LRG_259:g.4826del

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.1:c.-277del ENSP00000482169.1:n.-277del
NM_006158.4:c.-277del , LRG_259t1:c.-277del NP_006149.2:n.-277del
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