Canonical Allele Identifier: CA3306672

Gene: GFM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74741627A>T , CM000667.2:g.74741627A>T	GRCh38
NC_000005.9:g.74037452A>T , CM000667.1:g.74037452A>T	GRCh37
NC_000005.8:g.74073208A>T	NCBI36
NG_011531.1:g.30591T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032380.5:c.850-18T>A MANE Select	NP_115756.2:n.850-18T>A
ENST00000296805.8:c.850-18T>A MANE Select	ENSP00000296805.3:n.850-18T>A
NM_001281302.1:c.946-18T>A	NP_001268231.1:n.946-18T>A
NM_001281302.2:c.946-18T>A	NP_001268231.1:n.946-18T>A
NM_032380.4:c.850-18T>A	NP_115756.2:n.850-18T>A
NM_170681.2:c.850-18T>A	NP_733781.1:n.850-18T>A
NM_170681.3:c.850-18T>A	NP_733781.1:n.850-18T>A
NM_170691.2:c.850-18T>A	NP_733792.1:n.850-18T>A
NM_170691.3:c.850-18T>A	NP_733792.1:n.850-18T>A
NR_104006.1:n.1308-18T>A
NR_104006.2:n.1054-18T>A
ENST00000296805.7:c.850-18T>A	ENSP00000296805.3:n.850-18T>A
ENST00000345239.6:c.850-18T>A	ENSP00000296804.3:n.850-18T>A
ENST00000427854.6:c.850-18T>A	ENSP00000405808.2:n.850-18T>A
ENST00000509097.1:c.724-18T>A	ENSP00000421717.1:n.724-18T>A
ENST00000509430.5:c.850-18T>A	ENSP00000427004.1:n.850-18T>A
ENST00000513331.1:n.222T>A
XM_006714721.2:c.850-18T>A	XP_006714784.1:n.850-18T>A
XM_011543690.1:c.850-18T>A	XP_011541992.1:n.850-18T>A
XM_011543691.1:c.850-18T>A	XP_011541993.1:n.850-18T>A
XM_011543691.3:c.850-18T>A	XP_011541993.1:n.850-18T>A
XM_017009986.1:c.850-18T>A	XP_016865475.1:n.850-18T>A
XR_002956185.1:n.1084-18T>A