Canonical Allele Identifier: CA1771622029

Gene: NEFL

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24956563A= , CM000670.2:g.24956563A=	GRCh38
NC_000008.10:g.24814077A= , CM000670.1:g.24814077A=	GRCh37
NC_000008.9:g.24869994A=	NCBI36
NG_008492.1:g.5055T= , LRG_259:g.5055T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610854.2:c.-48T= MANE Select	ENSP00000482169.2:n.-48T=
ENST00000610854.1:c.-48T=	ENSP00000482169.1:n.-48T=
ENST00000615973.1:n.159T=
ENST00000619417.1:c.-48T=	ENSP00000483690.1:n.-48T=
NM_006158.4:c.-48T= , LRG_259t1:c.-48T=	NP_006149.2:n.-48T=
NM_006158.5:c.-48T= MANE Select	NP_006149.2:n.-48T=