Canonical Allele Identifier: CA355175806

Gene: GFM1 LXN

Linked Data

• COSMIC: COSM3846628
• MyVariant Identifiers: chr3:g.158364565C>T (hg19) ; chr3:g.158646776C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158646776C>T , CM000665.2:g.158646776C>T	GRCh38
NC_000003.11:g.158364565C>T , CM000665.1:g.158364565C>T	GRCh37
NC_000003.10:g.159847259C>T	NCBI36
NG_008441.1:g.7249C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486715.6:c.401C>T (GFM1) MANE Select	ENSP00000419038.1:p.Ala134Val
ENST00000264263.9:c.401C>T (GFM1)	ENSP00000264263.5:p.Ala134Val
ENST00000464732.1:c.176C>T (GFM1)	ENSP00000417532.1:p.Ala59Val
ENST00000478254.5:c.401C>T (GFM1)	ENSP00000417225.1:p.Ala134Val
ENST00000478576.5:c.401C>T (GFM1)	ENSP00000418755.1:p.Ala134Val
ENST00000482640.5:c.362-567G>A (LXN)
ENST00000486715.5:c.401C>T (GFM1)	ENSP00000419038.1:p.Ala134Val
NM_001308164.1:c.401C>T (GFM1)	NP_001295093.1:p.Ala134Val
NM_001308166.1:c.401C>T (GFM1)	NP_001295095.1:p.Ala134Val
NM_024996.5:c.401C>T (GFM1)	NP_079272.4:p.Ala134Val
XM_006713795.1:c.401C>T (GFM1)	XP_006713858.1:p.Ala134Val
XM_006713795.2:c.401C>T (GFM1)	XP_006713858.1:p.Ala134Val
NM_001374355.1:c.401C>T (GFM1)	NP_001361284.1:p.Ala134Val
NM_001374356.1:c.401C>T (GFM1)	NP_001361285.1:p.Ala134Val
NM_001374357.1:c.176C>T (GFM1)	NP_001361286.1:p.Ala59Val
NM_001374358.1:c.234+995C>T (GFM1)	NP_001361287.1:n.234+995C>T
NM_001374359.1:c.5+995C>T (GFM1)	NP_001361288.1:n.5+995C>T
NM_001374360.1:c.5+995C>T (GFM1)	NP_001361289.1:n.5+995C>T
NM_001374361.1:c.5+995C>T (GFM1)	NP_001361290.1:n.5+995C>T
NM_024996.7:c.401C>T (GFM1) MANE Select	NP_079272.4:p.Ala134Val
NR_164499.1:n.509C>T (GFM1)
NR_164500.1:n.509C>T (GFM1)
NR_164501.1:n.342+995C>T (GFM1)
NR_164502.1:n.509C>T (GFM1)
NM_001308164.2:c.401C>T (GFM1)	NP_001295093.1:p.Ala134Val
NM_001308166.2:c.401C>T (GFM1)	NP_001295095.1:p.Ala134Val