Canonical Allele Identifier: CA2682381

Gene: GFM1 LXN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158649135A>G , CM000665.2:g.158649135A>G	GRCh38
NC_000003.11:g.158366924A>G , CM000665.1:g.158366924A>G	GRCh37
NC_000003.10:g.159849618A>G	NCBI36
NG_008441.1:g.9608A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486715.6:c.667A>G (GFM1) MANE Select	ENSP00000419038.1:p.Ile223Val
ENST00000264263.9:c.667A>G (GFM1)	ENSP00000264263.5:p.Ile223Val
ENST00000478251.1:n.155A>G (GFM1)
ENST00000478254.5:c.667A>G (GFM1)	ENSP00000417225.1:p.Ile223Val
ENST00000478576.5:c.667A>G (GFM1)	ENSP00000418755.1:p.Ile223Val
ENST00000482640.5:c.362-2926T>C (LXN)
ENST00000486715.5:c.667A>G (GFM1)	ENSP00000419038.1:p.Ile223Val
NM_001308164.1:c.667A>G (GFM1)	NP_001295093.1:p.Ile223Val
NM_001308166.1:c.667A>G (GFM1)	NP_001295095.1:p.Ile223Val
NM_024996.5:c.667A>G (GFM1)	NP_079272.4:p.Ile223Val
XM_006713795.1:c.572+2188A>G (GFM1)	XP_006713858.1:n.572+2188A>G
XM_006713795.2:c.572+2188A>G (GFM1)	XP_006713858.1:n.572+2188A>G
NM_001374355.1:c.667A>G (GFM1)	NP_001361284.1:p.Ile223Val
NM_001374356.1:c.572+2188A>G (GFM1)	NP_001361285.1:n.572+2188A>G
NM_001374357.1:c.442A>G (GFM1)	NP_001361286.1:p.Ile148Val
NM_001374358.1:c.235-2965A>G (GFM1)	NP_001361287.1:n.235-2965A>G
NM_001374359.1:c.100A>G (GFM1)	NP_001361288.1:p.Ile34Val
NM_001374360.1:c.100A>G (GFM1)	NP_001361289.1:p.Ile34Val
NM_001374361.1:c.6-2961A>G (GFM1)	NP_001361290.1:n.6-2961A>G
NM_024996.7:c.667A>G (GFM1) MANE Select	NP_079272.4:p.Ile223Val
NR_164499.1:n.775A>G (GFM1)
NR_164500.1:n.775A>G (GFM1)
NR_164501.1:n.343-2961A>G (GFM1)
NR_164502.1:n.680+2188A>G (GFM1)
NM_001308164.2:c.667A>G (GFM1)	NP_001295093.1:p.Ile223Val
NM_001308166.2:c.667A>G (GFM1)	NP_001295095.1:p.Ile223Val