Canonical Allele Identifier: CA355176801
Community Standard Title: NM_024996.7(GFM1):c.787C>T (p.Gln263Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.158652193C>T , CM000665.2:g.158652193C>T GRCh38
NC_000003.11:g.158369982C>T , CM000665.1:g.158369982C>T GRCh37
NC_000003.10:g.159852676C>T NCBI36
NG_008441.1:g.12666C>T

Transcript Alleles

HGVS Amino-acid Change
NM_024996.7:c.787C>T (GFM1) MANE Select NP_079272.4:p.Gln263Ter
ENST00000486715.6:c.787C>T (GFM1) MANE Select ENSP00000419038.1:p.Gln263Ter
NM_001308164.1:c.844C>T (GFM1) NP_001295093.1:p.Gln282Ter
NM_001308164.2:c.844C>T (GFM1) NP_001295093.1:p.Gln282Ter
NM_001308166.1:c.787C>T (GFM1) NP_001295095.1:p.Gln263Ter
NM_001308166.2:c.787C>T (GFM1) NP_001295095.1:p.Gln263Ter
NM_001374355.1:c.844C>T (GFM1) NP_001361284.1:p.Gln282Ter
NM_001374356.1:c.670C>T (GFM1) NP_001361285.1:p.Gln224Ter
NM_001374357.1:c.562C>T (GFM1) NP_001361286.1:p.Gln188Ter
NM_001374358.1:c.328C>T (GFM1) NP_001361287.1:p.Gln110Ter
NM_001374359.1:c.220C>T (GFM1) NP_001361288.1:p.Gln74Ter
NM_001374360.1:c.220C>T (GFM1) NP_001361289.1:p.Gln74Ter
NM_001374361.1:c.103C>T (GFM1) NP_001361290.1:p.Gln35Ter
NM_024996.5:c.787C>T (GFM1) NP_079272.4:p.Gln263Ter
NR_164499.1:n.895C>T (GFM1)
NR_164500.1:n.895C>T (GFM1)
NR_164501.1:n.440C>T (GFM1)
NR_164502.1:n.778C>T (GFM1)
ENST00000264263.9:c.844C>T (GFM1) ENSP00000264263.5:p.Gln282Ter
ENST00000478254.5:c.787C>T (GFM1) ENSP00000417225.1:p.Gln263Ter
ENST00000478576.5:c.787C>T (GFM1) ENSP00000418755.1:p.Gln263Ter
ENST00000482640.5:c.362-5984G>A (LXN)
ENST00000486715.5:c.787C>T (GFM1) ENSP00000419038.1:p.Gln263Ter
XM_006713795.1:c.670C>T (GFM1) XP_006713858.1:p.Gln224Ter
XM_006713795.2:c.670C>T (GFM1) XP_006713858.1:p.Gln224Ter