Canonical Allele Identifier: CA342752

Gene: G6PC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075780G>C , CM000679.2:g.44075780G>C	GRCh38
NC_000017.10:g.42153148G>C , CM000679.1:g.42153148G>C	GRCh37
NC_000017.9:g.39508674G>C	NCBI36
NG_015818.1:g.10051G>C , LRG_182:g.10051G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*615G>C	ENSP00000466983.1:n.*615G>C
ENST00000588558.6:c.*753G>C	ENSP00000467624.1:n.*753G>C
ENST00000590253.3:c.*71G>C	ENSP00000465111.2:n.*71G>C
ENST00000593115.2:c.*799G>C	ENSP00000466821.1:n.*799G>C
ENST00000696383.1:c.433G>C	ENSP00000512593.1:p.Gly145Arg
ENST00000696384.1:c.*338G>C	ENSP00000512594.1:n.*338G>C
ENST00000696385.1:c.*496G>C	ENSP00000512595.1:n.*496G>C
ENST00000696386.1:c.*71G>C	ENSP00000512596.1:n.*71G>C
ENST00000696387.1:c.*405G>C	ENSP00000512597.1:n.*405G>C
ENST00000696388.1:c.*624G>C	ENSP00000512598.1:n.*624G>C
ENST00000696389.1:c.*809G>C	ENSP00000512599.1:n.*809G>C
ENST00000696390.1:c.568G>C	ENSP00000512600.1:p.Gly190Arg
ENST00000696391.1:c.*634G>C	ENSP00000512601.1:n.*634G>C
ENST00000696392.1:c.778G>C	ENSP00000512602.1:p.Gly260Arg
ENST00000696393.1:c.778G>C	ENSP00000512603.1:p.Gly260Arg
ENST00000696405.1:c.677+329G>C	ENSP00000512607.1:n.677+329G>C
ENST00000269097.9:c.778G>C MANE Select	ENSP00000269097.3:p.Gly260Arg
ENST00000269097.8:c.778G>C	ENSP00000269097.3:p.Gly260Arg
ENST00000585361.5:c.*615G>C	ENSP00000466983.1:n.*615G>C
ENST00000588558.5:c.*753G>C	ENSP00000467624.1:n.*753G>C
ENST00000590253.2:c.280G>C
ENST00000590639.1:n.799G>C
ENST00000591696.1:c.670G>C	ENSP00000468677.1:p.Gly224Arg
NM_138387.3:c.778G>C , LRG_182t1:c.778G>C	NP_612396.1:p.Gly260Arg
NR_028581.1:n.1208G>C
NR_028582.1:n.1073G>C
XM_011525473.1:c.433G>C	XP_011523775.1:p.Gly145Arg
XM_011525474.1:c.433G>C	XP_011523776.1:p.Gly145Arg
NM_001319945.1:c.*71G>C	NP_001306874.1:n.*71G>C
XM_011525473.3:c.433G>C	XP_011523775.1:p.Gly145Arg
XM_011525474.3:c.433G>C	XP_011523776.1:p.Gly145Arg
XM_017025335.2:c.433G>C	XP_016880824.1:p.Gly145Arg
NM_001319945.2:c.*71G>C	NP_001306874.1:n.*71G>C
NR_028581.2:n.1027G>C
NR_028582.2:n.892G>C
NM_001384165.1:c.433G>C	NP_001371094.1:p.Gly145Arg
NM_001384166.1:c.433G>C	NP_001371095.1:p.Gly145Arg
NM_001384167.1:c.433G>C	NP_001371096.1:p.Gly145Arg
NM_001384168.1:c.433G>C	NP_001371097.1:p.Gly145Arg
NM_138387.4:c.778G>C MANE Select	NP_612396.1:p.Gly260Arg