Canonical Allele Identifier: CA355178464

Gene: GFM1 LXN

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.158665472C>T , CM000665.2:g.158665472C>T	GRCh38
NC_000003.11:g.158383261C>T , CM000665.1:g.158383261C>T	GRCh37
NC_000003.10:g.159865955C>T	NCBI36
NG_008441.1:g.25945C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024996.7:c.1516C>T (GFM1) MANE Select	NP_079272.4:p.Gln506Ter
ENST00000486715.6:c.1516C>T (GFM1) MANE Select	ENSP00000419038.1:p.Gln506Ter
NM_001308164.1:c.1573C>T (GFM1)	NP_001295093.1:p.Gln525Ter
NM_001308164.2:c.1573C>T (GFM1)	NP_001295093.1:p.Gln525Ter
NM_001308166.1:c.1516C>T (GFM1)	NP_001295095.1:p.Gln506Ter
NM_001308166.2:c.1516C>T (GFM1)	NP_001295095.1:p.Gln506Ter
NM_001374355.1:c.1435C>T (GFM1)	NP_001361284.1:p.Gln479Ter
NM_001374356.1:c.1399C>T (GFM1)	NP_001361285.1:p.Gln467Ter
NM_001374357.1:c.1291C>T (GFM1)	NP_001361286.1:p.Gln431Ter
NM_001374358.1:c.1057C>T (GFM1)	NP_001361287.1:p.Gln353Ter
NM_001374359.1:c.949C>T (GFM1)	NP_001361288.1:p.Gln317Ter
NM_001374360.1:c.949C>T (GFM1)	NP_001361289.1:p.Gln317Ter
NM_001374361.1:c.832C>T (GFM1)	NP_001361290.1:p.Gln278Ter
NM_024996.5:c.1516C>T (GFM1)	NP_079272.4:p.Gln506Ter
NR_164499.1:n.1539C>T (GFM1)
NR_164500.1:n.1624C>T (GFM1)
NR_164501.1:n.1169C>T (GFM1)
NR_164502.1:n.1503C>T (GFM1)
ENST00000264263.9:c.1573C>T (GFM1)	ENSP00000264263.5:p.Gln525Ter
ENST00000478254.5:c.*156C>T (GFM1)	ENSP00000417225.1:n.*156C>T
ENST00000478576.5:c.1516C>T (GFM1)	ENSP00000418755.1:p.Gln506Ter
ENST00000482640.5:c.361+1540G>A (LXN)
ENST00000486715.5:c.1516C>T (GFM1)	ENSP00000419038.1:p.Gln506Ter
XM_006713795.1:c.1399C>T (GFM1)	XP_006713858.1:p.Gln467Ter
XM_006713795.2:c.1399C>T (GFM1)	XP_006713858.1:p.Gln467Ter