Canonical Allele Identifier: CA1771650656

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24952456G= , CM000670.2:g.24952456G=	GRCh38
NC_000008.10:g.24809969G= , CM000670.1:g.24809969G=	GRCh37
NC_000008.9:g.24865886G=	NCBI36
NG_008492.1:g.9162C= , LRG_259:g.9162C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610854.2:c.*354C= MANE Select	ENSP00000482169.2:n.*354C=
ENST00000610854.1:c.*354C=	ENSP00000482169.1:n.*354C=
ENST00000619417.1:c.*851C=	ENSP00000483690.1:n.*851C=
NM_006158.4:c.*354C= , LRG_259t1:c.*354C=	NP_006149.2:n.*354C=
NM_006158.5:c.*354C= MANE Select	NP_006149.2:n.*354C=