Canonical Allele Identifier: CA3796917

Gene: LRFN2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.40432255C>T , CM000668.2:g.40432255C>T	GRCh38
NC_000006.11:g.40399994C>T , CM000668.1:g.40399994C>T	GRCh37
NC_000006.10:g.40507972C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_020737.3:c.859G>A MANE Select	NP_065788.1:p.Glu287Lys
ENST00000338305.7:c.859G>A MANE Select	ENSP00000345985.6:p.Glu287Lys
NM_020737.2:c.859G>A	NP_065788.1:p.Glu287Lys
ENST00000338305.6:c.859G>A	ENSP00000345985.6:p.Glu287Lys
ENST00000700335.1:c.859G>A	ENSP00000514953.1:p.Glu287Lys
XM_011514759.1:c.985G>A	XP_011513061.1:p.Glu329Lys
XM_011514760.1:c.985G>A	XP_011513062.1:p.Glu329Lys
XM_011514761.1:c.859G>A	XP_011513063.1:p.Glu287Lys
XM_011514761.2:c.859G>A	XP_011513063.1:p.Glu287Lys
XM_011514762.1:c.859G>A	XP_011513064.1:p.Glu287Lys
XM_011514762.2:c.859G>A	XP_011513064.1:p.Glu287Lys
XM_011514763.1:c.859G>A	XP_011513065.1:p.Glu287Lys
XM_017011110.1:c.859G>A	XP_016866599.1:p.Glu287Lys
XM_017011111.1:c.859G>A	XP_016866600.1:p.Glu287Lys