Canonical Allele Identifier: CA1771650990

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24952660T= , CM000670.2:g.24952660T=	GRCh38
NC_000008.10:g.24810173T= , CM000670.1:g.24810173T=	GRCh37
NC_000008.9:g.24866090T=	NCBI36
NG_008492.1:g.8958A= , LRG_259:g.8958A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610854.2:c.*150A= MANE Select	ENSP00000482169.2:n.*150A=
ENST00000610854.1:c.*150A=	ENSP00000482169.1:n.*150A=
ENST00000619417.1:c.*647A=	ENSP00000483690.1:n.*647A=
NM_006158.4:c.*150A= , LRG_259t1:c.*150A=	NP_006149.2:n.*150A=
NM_006158.5:c.*150A= MANE Select	NP_006149.2:n.*150A=