Canonical Allele Identifier: CA1771621648

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24956458C= , CM000670.2:g.24956458C=	GRCh38
NC_000008.10:g.24813972C= , CM000670.1:g.24813972C=	GRCh37
NC_000008.9:g.24869889C=	NCBI36
NG_008492.1:g.5160G= , LRG_259:g.5160G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000610854.2:c.58G= MANE Select	ENSP00000482169.2:p.Glu20=
ENST00000610854.1:c.58G=	ENSP00000482169.1:p.Glu20=
ENST00000615973.1:n.264G=
ENST00000619417.1:c.58G=	ENSP00000483690.1:p.Glu20=
NM_006158.4:c.58G= , LRG_259t1:c.58G=	NP_006149.2:p.Glu20=
NM_006158.5:c.58G= MANE Select	NP_006149.2:p.Glu20=