Canonical Allele Identifier: CA399729263

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42153127C>A (hg19) ; chr17:g.44075759C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075759C>A , CM000679.2:g.44075759C>A	GRCh38
NC_000017.10:g.42153127C>A , CM000679.1:g.42153127C>A	GRCh37
NC_000017.9:g.39508653C>A	NCBI36
NG_015818.1:g.10030C>A , LRG_182:g.10030C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*594C>A	ENSP00000466983.1:n.*594C>A
ENST00000588558.6:c.*732C>A	ENSP00000467624.1:n.*732C>A
ENST00000590253.3:c.*50C>A	ENSP00000465111.2:n.*50C>A
ENST00000593115.2:c.*778C>A	ENSP00000466821.1:n.*778C>A
ENST00000696383.1:c.412C>A	ENSP00000512593.1:p.Arg138Ser
ENST00000696384.1:c.*317C>A	ENSP00000512594.1:n.*317C>A
ENST00000696385.1:c.*475C>A	ENSP00000512595.1:n.*475C>A
ENST00000696386.1:c.*50C>A	ENSP00000512596.1:n.*50C>A
ENST00000696387.1:c.*384C>A	ENSP00000512597.1:n.*384C>A
ENST00000696388.1:c.*603C>A	ENSP00000512598.1:n.*603C>A
ENST00000696389.1:c.*788C>A	ENSP00000512599.1:n.*788C>A
ENST00000696390.1:c.547C>A	ENSP00000512600.1:p.Arg183Ser
ENST00000696391.1:c.*613C>A	ENSP00000512601.1:n.*613C>A
ENST00000696392.1:c.757C>A	ENSP00000512602.1:p.Arg253Ser
ENST00000696393.1:c.757C>A	ENSP00000512603.1:p.Arg253Ser
ENST00000696405.1:c.677+308C>A	ENSP00000512607.1:n.677+308C>A
ENST00000269097.9:c.757C>A MANE Select	ENSP00000269097.3:p.Arg253Ser
ENST00000269097.8:c.757C>A	ENSP00000269097.3:p.Arg253Ser
ENST00000585361.5:c.*594C>A	ENSP00000466983.1:n.*594C>A
ENST00000588558.5:c.*732C>A	ENSP00000467624.1:n.*732C>A
ENST00000590253.2:c.259C>A
ENST00000590639.1:n.778C>A
ENST00000591696.1:c.649C>A	ENSP00000468677.1:p.Arg217Ser
NM_138387.3:c.757C>A , LRG_182t1:c.757C>A	NP_612396.1:p.Arg253Ser
NR_028581.1:n.1187C>A
NR_028582.1:n.1052C>A
XM_011525473.1:c.412C>A	XP_011523775.1:p.Arg138Ser
XM_011525474.1:c.412C>A	XP_011523776.1:p.Arg138Ser
NM_001319945.1:c.*50C>A	NP_001306874.1:n.*50C>A
XM_011525473.3:c.412C>A	XP_011523775.1:p.Arg138Ser
XM_011525474.3:c.412C>A	XP_011523776.1:p.Arg138Ser
XM_017025335.2:c.412C>A	XP_016880824.1:p.Arg138Ser
NM_001319945.2:c.*50C>A	NP_001306874.1:n.*50C>A
NR_028581.2:n.1006C>A
NR_028582.2:n.871C>A
NM_001384165.1:c.412C>A	NP_001371094.1:p.Arg138Ser
NM_001384166.1:c.412C>A	NP_001371095.1:p.Arg138Ser
NM_001384167.1:c.412C>A	NP_001371096.1:p.Arg138Ser
NM_001384168.1:c.412C>A	NP_001371097.1:p.Arg138Ser
NM_138387.4:c.757C>A MANE Select	NP_612396.1:p.Arg253Ser