Canonical Allele Identifier: CA1771650649

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24952447G= , CM000670.2:g.24952447G=	GRCh38
NC_000008.10:g.24809960G= , CM000670.1:g.24809960G=	GRCh37
NC_000008.9:g.24865877G=	NCBI36
NG_008492.1:g.9171C= , LRG_259:g.9171C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000610854.2:c.*363C= MANE Select	ENSP00000482169.2:n.*363C=
ENST00000610854.1:c.*363C=	ENSP00000482169.1:n.*363C=
ENST00000619417.1:c.*860C=	ENSP00000483690.1:n.*860C=
NM_006158.4:c.*363C= , LRG_259t1:c.*363C=	NP_006149.2:n.*363C=
NM_006158.5:c.*363C= MANE Select	NP_006149.2:n.*363C=