Canonical Allele Identifier: CA1771622066

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24956589G= , CM000670.2:g.24956589G=	GRCh38
NC_000008.10:g.24814103G= , CM000670.1:g.24814103G=	GRCh37
NC_000008.9:g.24870020G=	NCBI36
NG_008492.1:g.5029C= , LRG_259:g.5029C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610854.2:c.-74C= MANE Select	ENSP00000482169.2:n.-74C=
ENST00000610854.1:c.-74C=	ENSP00000482169.1:n.-74C=
ENST00000615973.1:n.133C=
ENST00000619417.1:c.-74C=	ENSP00000483690.1:n.-74C=
NM_006158.4:c.-74C= , LRG_259t1:c.-74C=	NP_006149.2:n.-74C=
NM_006158.5:c.-74C= MANE Select	NP_006149.2:n.-74C=