Canonical Allele Identifier: CA500616861

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42152724G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075356G>C , CM000679.2:g.44075356G>C	GRCh38
NC_000017.10:g.42152724G>C , CM000679.1:g.42152724G>C	GRCh37
NC_000017.9:g.39508250G>C	NCBI36
NG_015818.1:g.9627G>C , LRG_182:g.9627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*419G>C	ENSP00000466983.1:n.*419G>C
ENST00000588558.6:c.*557G>C	ENSP00000467624.1:n.*557G>C
ENST00000590253.3:c.463G>C	ENSP00000465111.2:p.Gly155Arg
ENST00000593115.2:c.*603G>C	ENSP00000466821.1:n.*603G>C
ENST00000696383.1:c.237G>C	ENSP00000512593.1:p.Arg79=
ENST00000696384.1:c.*142G>C	ENSP00000512594.1:n.*142G>C
ENST00000696385.1:c.*300G>C	ENSP00000512595.1:n.*300G>C
ENST00000696386.1:c.265G>C	ENSP00000512596.1:p.Gly89Arg
ENST00000696387.1:c.*209G>C	ENSP00000512597.1:n.*209G>C
ENST00000696388.1:c.*428G>C	ENSP00000512598.1:n.*428G>C
ENST00000696389.1:c.*613G>C	ENSP00000512599.1:n.*613G>C
ENST00000696390.1:c.372G>C	ENSP00000512600.1:p.Arg124=
ENST00000696391.1:c.*438G>C	ENSP00000512601.1:n.*438G>C
ENST00000696392.1:c.582G>C	ENSP00000512602.1:p.Arg194=
ENST00000696393.1:c.582G>C	ENSP00000512603.1:p.Arg194=
ENST00000696405.1:c.582G>C	ENSP00000512607.1:p.Arg194=
ENST00000269097.9:c.582G>C MANE Select	ENSP00000269097.3:p.Arg194=
ENST00000269097.8:c.582G>C	ENSP00000269097.3:p.Arg194=
ENST00000585361.5:c.*419G>C	ENSP00000466983.1:n.*419G>C
ENST00000588558.5:c.*557G>C	ENSP00000467624.1:n.*557G>C
ENST00000590253.2:c.84G>C
ENST00000590639.1:n.603G>C
ENST00000591696.1:c.474G>C	ENSP00000468677.1:p.Arg158=
NM_138387.3:c.582G>C , LRG_182t1:c.582G>C	NP_612396.1:p.Arg194=
NR_028581.1:n.1012G>C
NR_028582.1:n.877G>C
XM_006722179.2:c.463G>C	XP_006722242.1:p.Gly155Arg
XM_011525473.1:c.237G>C	XP_011523775.1:p.Arg79=
XM_011525474.1:c.237G>C	XP_011523776.1:p.Arg79=
NM_001319945.1:c.463G>C	NP_001306874.1:p.Gly155Arg
XM_011525473.3:c.237G>C	XP_011523775.1:p.Arg79=
XM_011525474.3:c.237G>C	XP_011523776.1:p.Arg79=
XM_017025335.2:c.237G>C	XP_016880824.1:p.Arg79=
NM_001319945.2:c.463G>C	NP_001306874.1:p.Gly155Arg
NR_028581.2:n.831G>C
NR_028582.2:n.696G>C
NM_001384165.1:c.237G>C	NP_001371094.1:p.Arg79=
NM_001384166.1:c.237G>C	NP_001371095.1:p.Arg79=
NM_001384167.1:c.237G>C	NP_001371096.1:p.Arg79=
NM_001384168.1:c.237G>C	NP_001371097.1:p.Arg79=
NM_138387.4:c.582G>C MANE Select	NP_612396.1:p.Arg194=