Canonical Allele Identifier: CA436482172

Gene: GFM1 LXN

Linked Data

• MyVariant Identifiers: chr3:g.158364533G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158646744G>T , CM000665.2:g.158646744G>T	GRCh38
NC_000003.11:g.158364533G>T , CM000665.1:g.158364533G>T	GRCh37
NC_000003.10:g.159847227G>T	NCBI36
NG_008441.1:g.7217G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486715.6:c.369G>T (GFM1) MANE Select	ENSP00000419038.1:p.Gly123=
ENST00000264263.9:c.369G>T (GFM1)	ENSP00000264263.5:p.Gly123=
ENST00000464732.1:c.144G>T (GFM1)	ENSP00000417532.1:p.Gly48=
ENST00000478254.5:c.369G>T (GFM1)	ENSP00000417225.1:p.Gly123=
ENST00000478576.5:c.369G>T (GFM1)	ENSP00000418755.1:p.Gly123=
ENST00000482640.5:c.362-535C>A (LXN)
ENST00000486715.5:c.369G>T (GFM1)	ENSP00000419038.1:p.Gly123=
NM_001308164.1:c.369G>T (GFM1)	NP_001295093.1:p.Gly123=
NM_001308166.1:c.369G>T (GFM1)	NP_001295095.1:p.Gly123=
NM_024996.5:c.369G>T (GFM1)	NP_079272.4:p.Gly123=
XM_006713795.1:c.369G>T (GFM1)	XP_006713858.1:p.Gly123=
XM_006713795.2:c.369G>T (GFM1)	XP_006713858.1:p.Gly123=
NM_001374355.1:c.369G>T (GFM1)	NP_001361284.1:p.Gly123=
NM_001374356.1:c.369G>T (GFM1)	NP_001361285.1:p.Gly123=
NM_001374357.1:c.144G>T (GFM1)	NP_001361286.1:p.Gly48=
NM_001374358.1:c.234+963G>T (GFM1)	NP_001361287.1:n.234+963G>T
NM_001374359.1:c.5+963G>T (GFM1)	NP_001361288.1:n.5+963G>T
NM_001374360.1:c.5+963G>T (GFM1)	NP_001361289.1:n.5+963G>T
NM_001374361.1:c.5+963G>T (GFM1)	NP_001361290.1:n.5+963G>T
NM_024996.7:c.369G>T (GFM1) MANE Select	NP_079272.4:p.Gly123=
NR_164499.1:n.477G>T (GFM1)
NR_164500.1:n.477G>T (GFM1)
NR_164501.1:n.342+963G>T (GFM1)
NR_164502.1:n.477G>T (GFM1)
NM_001308164.2:c.369G>T (GFM1)	NP_001295093.1:p.Gly123=
NM_001308166.2:c.369G>T (GFM1)	NP_001295095.1:p.Gly123=