Canonical Allele Identifier: CA1771621659

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24956461C= , CM000670.2:g.24956461C=	GRCh38
NC_000008.10:g.24813975C= , CM000670.1:g.24813975C=	GRCh37
NC_000008.9:g.24869892C=	NCBI36
NG_008492.1:g.5157G= , LRG_259:g.5157G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610854.2:c.55G= MANE Select	ENSP00000482169.2:p.Val19=
ENST00000610854.1:c.55G=	ENSP00000482169.1:p.Val19=
ENST00000615973.1:n.261G=
ENST00000619417.1:c.55G=	ENSP00000483690.1:p.Val19=
NM_006158.4:c.55G= , LRG_259t1:c.55G=	NP_006149.2:p.Val19=
NM_006158.5:c.55G= MANE Select	NP_006149.2:p.Val19=