Canonical Allele Identifier: CA370623961
Gene: NEFL HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.24813908G>T (hg19) chr8:g.24956394G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956394G>T , CM000670.2:g.24956394G>T GRCh38
NC_000008.10:g.24813908G>T , CM000670.1:g.24813908G>T GRCh37
NC_000008.9:g.24869825G>T NCBI36
NG_008492.1:g.5224C>A , LRG_259:g.5224C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000610854.2:c.122C>A MANE Select ENSP00000482169.2:p.Ser41Tyr
ENST00000610854.1:c.122C>A ENSP00000482169.1:p.Ser41Tyr
ENST00000615973.1:n.328C>A
ENST00000619417.1:c.122C>A ENSP00000483690.1:p.Ser41Tyr
NM_006158.4:c.122C>A , LRG_259t1:c.122C>A NP_006149.2:p.Ser41Tyr
NM_006158.5:c.122C>A MANE Select NP_006149.2:p.Ser41Tyr
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