Canonical Allele Identifier: CA1771621662
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956462G= , CM000670.2:g.24956462G= GRCh38
NC_000008.10:g.24813976G= , CM000670.1:g.24813976G= GRCh37
NC_000008.9:g.24869893G= NCBI36
NG_008492.1:g.5156C= , LRG_259:g.5156C=

Transcript Alleles

HGVS Amino-acid change
ENST00000610854.2:c.54C= MANE Select ENSP00000482169.2:p.Tyr18=
ENST00000610854.1:c.54C= ENSP00000482169.1:p.Tyr18=
ENST00000615973.1:n.260C=
ENST00000619417.1:c.54C= ENSP00000483690.1:p.Tyr18=
NM_006158.4:c.54C= , LRG_259t1:c.54C= NP_006149.2:p.Tyr18=
NM_006158.5:c.54C= MANE Select NP_006149.2:p.Tyr18=