Canonical Allele Identifier: CA1555784360

Gene: GFM2 HEXB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74721740G= , CM000667.2:g.74721740G=	GRCh38
NC_000005.9:g.74017565G= , CM000667.1:g.74017565G=	GRCh37
NC_000005.8:g.74053321G=	NCBI36
NG_009770.1:g.41597G=
NG_011531.1:g.50478C=
NG_009770.2:g.86718G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2255C= (GFM2) MANE Select	ENSP00000296805.3:p.Thr752=
ENST00000296805.7:c.2255C= (GFM2)	ENSP00000296805.3:p.Thr752=
ENST00000345239.6:c.2114C= (GFM2)	ENSP00000296804.3:p.Thr705=
ENST00000503312.5:c.608+304G= (HEXB)
ENST00000505859.1:c.255+304G= (HEXB)
ENST00000509430.5:c.2255C= (GFM2)	ENSP00000427004.1:p.Thr752=
ENST00000513867.1:n.380+304G= (HEXB)
ENST00000515125.5:n.658C= (GFM2)
NM_001281302.1:c.2351C= (GFM2)	NP_001268231.1:p.Thr784=
NM_032380.4:c.2255C= (GFM2)	NP_115756.2:p.Thr752=
NM_170691.2:c.2114C= (GFM2)	NP_733792.1:p.Thr705=
NR_104006.1:n.2574C= (GFM2)
XM_006714721.2:c.2120C= (GFM2)	XP_006714784.1:p.Thr707=
XM_011543690.1:c.2255C= (GFM2)	XP_011541992.1:p.Thr752=
XM_017009986.1:c.2255C= (GFM2)	XP_016865475.1:p.Thr752=
XR_002956185.1:n.3541C= (GFM2)
NM_032380.5:c.2255C= (GFM2) MANE Select	NP_115756.2:p.Thr752=
NM_001281302.2:c.2351C= (GFM2)	NP_001268231.1:p.Thr784=
NM_170691.3:c.2114C= (GFM2)	NP_733792.1:p.Thr705=
NR_104006.2:n.2320C= (GFM2)