Canonical Allele Identifier: CA1414370131

Gene: GFM1 LXN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158649001G= , CM000665.2:g.158649001G=	GRCh38
NC_000003.11:g.158366790G= , CM000665.1:g.158366790G=	GRCh37
NC_000003.10:g.159849484G=	NCBI36
NG_008441.1:g.9474G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000486715.6:c.573-40G= (GFM1) MANE Select	ENSP00000419038.1:n.573-40G=
ENST00000264263.9:c.573-40G= (GFM1)	ENSP00000264263.5:n.573-40G=
ENST00000478251.1:n.61-40G= (GFM1)
ENST00000478254.5:c.573-40G= (GFM1)	ENSP00000417225.1:n.573-40G=
ENST00000478576.5:c.573-40G= (GFM1)	ENSP00000418755.1:n.573-40G=
ENST00000482640.5:c.362-2792C= (LXN)
ENST00000486715.5:c.573-40G= (GFM1)	ENSP00000419038.1:n.573-40G=
NM_001308164.1:c.573-40G= (GFM1)	NP_001295093.1:n.573-40G=
NM_001308166.1:c.573-40G= (GFM1)	NP_001295095.1:n.573-40G=
NM_024996.5:c.573-40G= (GFM1)	NP_079272.4:n.573-40G=
XM_006713795.1:c.572+2054G= (GFM1)	XP_006713858.1:n.572+2054G=
XM_006713795.2:c.572+2054G= (GFM1)	XP_006713858.1:n.572+2054G=
NM_001374355.1:c.573-40G= (GFM1)	NP_001361284.1:n.573-40G=
NM_001374356.1:c.572+2054G= (GFM1)	NP_001361285.1:n.572+2054G=
NM_001374357.1:c.348-40G= (GFM1)	NP_001361286.1:n.348-40G=
NM_001374358.1:c.235-3099G= (GFM1)	NP_001361287.1:n.235-3099G=
NM_001374359.1:c.6-40G= (GFM1)	NP_001361288.1:n.6-40G=
NM_001374360.1:c.6-40G= (GFM1)	NP_001361289.1:n.6-40G=
NM_001374361.1:c.6-3095G= (GFM1)	NP_001361290.1:n.6-3095G=
NM_024996.7:c.573-40G= (GFM1) MANE Select	NP_079272.4:n.573-40G=
NR_164499.1:n.681-40G= (GFM1)
NR_164500.1:n.681-40G= (GFM1)
NR_164501.1:n.343-3095G= (GFM1)
NR_164502.1:n.680+2054G= (GFM1)
NM_001308164.2:c.573-40G= (GFM1)	NP_001295093.1:n.573-40G=
NM_001308166.2:c.573-40G= (GFM1)	NP_001295095.1:n.573-40G=