Canonical Allele Identifier: CA460021352

Gene: NEFL

Linked Data

• MyVariant Identifiers: chr8:g.24814172C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.24956658C>A , CM000670.2:g.24956658C>A	GRCh38
NC_000008.10:g.24814172C>A , CM000670.1:g.24814172C>A	GRCh37
NC_000008.9:g.24870089C>A	NCBI36
NG_008492.1:g.4960G>T , LRG_259:g.4960G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000610854.1:c.-143G>T	ENSP00000482169.1:n.-143G>T
ENST00000615973.1:n.64G>T
NM_006158.4:c.-143G>T , LRG_259t1:c.-143G>T	NP_006149.2:n.-143G>T