Canonical Allele Identifier: CA1771622100

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24956606T= , CM000670.2:g.24956606T=	GRCh38
NC_000008.10:g.24814120T= , CM000670.1:g.24814120T=	GRCh37
NC_000008.9:g.24870037T=	NCBI36
NG_008492.1:g.5012A= , LRG_259:g.5012A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610854.2:c.-91A= MANE Select	ENSP00000482169.2:n.-91A=
ENST00000610854.1:c.-91A=	ENSP00000482169.1:n.-91A=
ENST00000615973.1:n.116A=
ENST00000619417.1:c.-91A=	ENSP00000483690.1:n.-91A=
NM_006158.4:c.-91A= , LRG_259t1:c.-91A=	NP_006149.2:n.-91A=
NM_006158.5:c.-91A= MANE Select	NP_006149.2:n.-91A=