Canonical Allele Identifier: CA1555786017

Gene: GFM2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74725636A= , CM000667.2:g.74725636A=	GRCh38
NC_000005.9:g.74021461A= , CM000667.1:g.74021461A=	GRCh37
NC_000005.8:g.74057217A=	NCBI36
NG_011531.1:g.46582T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296805.8:c.2028+4T= MANE Select	ENSP00000296805.3:n.2028+4T=
ENST00000296805.7:c.2028+4T=	ENSP00000296805.3:n.2028+4T=
ENST00000345239.6:c.1887+4T=	ENSP00000296804.3:n.1887+4T=
ENST00000509430.5:c.2028+4T=	ENSP00000427004.1:n.2028+4T=
ENST00000515125.5:n.431+305T=
NM_001281302.1:c.2124+4T=	NP_001268231.1:n.2124+4T=
NM_032380.4:c.2028+4T=	NP_115756.2:n.2028+4T=
NM_170691.2:c.1887+4T=	NP_733792.1:n.1887+4T=
NR_104006.1:n.2347+4T=
XM_006714721.2:c.1893+4T=	XP_006714784.1:n.1893+4T=
XM_011543690.1:c.2028+4T=	XP_011541992.1:n.2028+4T=
XM_017009986.1:c.2028+4T=	XP_016865475.1:n.2028+4T=
XR_002956185.1:n.3314+4T=
NM_032380.5:c.2028+4T= MANE Select	NP_115756.2:n.2028+4T=
NM_001281302.2:c.2124+4T=	NP_001268231.1:n.2124+4T=
NM_170691.3:c.1887+4T=	NP_733792.1:n.1887+4T=
NR_104006.2:n.2093+4T=