Canonical Allele Identifier: CA324909

Gene: GFM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725684A>T , CM000667.2:g.74725684A>T	GRCh38
NC_000005.9:g.74021509A>T , CM000667.1:g.74021509A>T	GRCh37
NC_000005.8:g.74057265A>T	NCBI36
NG_011531.1:g.46534T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.1984T>A MANE Select	ENSP00000296805.3:p.Ser662Thr
ENST00000296805.7:c.1984T>A	ENSP00000296805.3:p.Ser662Thr
ENST00000345239.6:c.1843T>A	ENSP00000296804.3:p.Ser615Thr
ENST00000509430.5:c.1984T>A	ENSP00000427004.1:p.Ser662Thr
ENST00000514734.5:n.895T>A
ENST00000515125.5:n.431+257T>A
NM_001281302.1:c.2080T>A	NP_001268231.1:p.Ser694Thr
NM_032380.4:c.1984T>A	NP_115756.2:p.Ser662Thr
NM_170691.2:c.1843T>A	NP_733792.1:p.Ser615Thr
NR_104006.1:n.2303T>A
XM_006714721.2:c.1849T>A	XP_006714784.1:p.Ser617Thr
XM_011543690.1:c.1984T>A	XP_011541992.1:p.Ser662Thr
XM_017009986.1:c.1984T>A	XP_016865475.1:p.Ser662Thr
XR_002956185.1:n.3270T>A
NM_032380.5:c.1984T>A MANE Select	NP_115756.2:p.Ser662Thr
NM_001281302.2:c.2080T>A	NP_001268231.1:p.Ser694Thr
NM_170691.3:c.1843T>A	NP_733792.1:p.Ser615Thr
NR_104006.2:n.2049T>A