Canonical Allele Identifier: CA1771621625
Gene: NEFL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.24956453C= , CM000670.2:g.24956453C= GRCh38
NC_000008.10:g.24813967C= , CM000670.1:g.24813967C= GRCh37
NC_000008.9:g.24869884C= NCBI36
NG_008492.1:g.5165G= , LRG_259:g.5165G=

Transcript Alleles

HGVS Amino-acid change
ENST00000610854.2:c.63G= MANE Select ENSP00000482169.2:p.Thr21=
ENST00000610854.1:c.63G= ENSP00000482169.1:p.Thr21=
ENST00000615973.1:n.269G=
ENST00000619417.1:c.63G= ENSP00000483690.1:p.Thr21=
NM_006158.4:c.63G= , LRG_259t1:c.63G= NP_006149.2:p.Thr21=
NM_006158.5:c.63G= MANE Select NP_006149.2:p.Thr21=