Canonical Allele Identifier: CA1771621665

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24956463T= , CM000670.2:g.24956463T=	GRCh38
NC_000008.10:g.24813977T= , CM000670.1:g.24813977T=	GRCh37
NC_000008.9:g.24869894T=	NCBI36
NG_008492.1:g.5155A= , LRG_259:g.5155A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000610854.2:c.53A= MANE Select	ENSP00000482169.2:p.Tyr18=
ENST00000610854.1:c.53A=	ENSP00000482169.1:p.Tyr18=
ENST00000615973.1:n.259A=
ENST00000619417.1:c.53A=	ENSP00000483690.1:p.Tyr18=
NM_006158.4:c.53A= , LRG_259t1:c.53A=	NP_006149.2:p.Tyr18=
NM_006158.5:c.53A= MANE Select	NP_006149.2:p.Tyr18=