Canonical Allele Identifier: CA1555784395

Gene: GFM2 HEXB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74721814A= , CM000667.2:g.74721814A=	GRCh38
NC_000005.9:g.74017639A= , CM000667.1:g.74017639A=	GRCh37
NC_000005.8:g.74053395A=	NCBI36
NG_009770.1:g.41671A=
NG_011531.1:g.50404T=
NG_009770.2:g.86792A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2212-31T= (GFM2) MANE Select	ENSP00000296805.3:n.2212-31T=
ENST00000296805.7:c.2212-31T= (GFM2)	ENSP00000296805.3:n.2212-31T=
ENST00000345239.6:c.2071-31T= (GFM2)	ENSP00000296804.3:n.2071-31T=
ENST00000503312.5:c.608+378A= (HEXB)
ENST00000505859.1:c.255+378A= (HEXB)
ENST00000509430.5:c.2212-31T= (GFM2)	ENSP00000427004.1:n.2212-31T=
ENST00000513867.1:n.380+378A= (HEXB)
ENST00000515125.5:n.615-31T= (GFM2)
NM_001281302.1:c.2308-31T= (GFM2)	NP_001268231.1:n.2308-31T=
NM_032380.4:c.2212-31T= (GFM2)	NP_115756.2:n.2212-31T=
NM_170691.2:c.2071-31T= (GFM2)	NP_733792.1:n.2071-31T=
NR_104006.1:n.2531-31T= (GFM2)
XM_006714721.2:c.2077-31T= (GFM2)	XP_006714784.1:n.2077-31T=
XM_011543690.1:c.2212-31T= (GFM2)	XP_011541992.1:n.2212-31T=
XM_017009986.1:c.2212-31T= (GFM2)	XP_016865475.1:n.2212-31T=
XR_002956185.1:n.3498-31T= (GFM2)
NM_032380.5:c.2212-31T= (GFM2) MANE Select	NP_115756.2:n.2212-31T=
NM_001281302.2:c.2308-31T= (GFM2)	NP_001268231.1:n.2308-31T=
NM_170691.3:c.2071-31T= (GFM2)	NP_733792.1:n.2071-31T=
NR_104006.2:n.2277-31T= (GFM2)