Canonical Allele Identifier: CA500243263

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42152679C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075311C>G , CM000679.2:g.44075311C>G	GRCh38
NC_000017.10:g.42152679C>G , CM000679.1:g.42152679C>G	GRCh37
NC_000017.9:g.39508205C>G	NCBI36
NG_015818.1:g.9582C>G , LRG_182:g.9582C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*374C>G	ENSP00000466983.1:n.*374C>G
ENST00000588558.6:c.*512C>G	ENSP00000467624.1:n.*512C>G
ENST00000590253.3:c.418C>G	ENSP00000465111.2:p.Arg140Gly
ENST00000593115.2:c.*558C>G	ENSP00000466821.1:n.*558C>G
ENST00000696383.1:c.192C>G	ENSP00000512593.1:p.Gly64=
ENST00000696384.1:c.*97C>G	ENSP00000512594.1:n.*97C>G
ENST00000696385.1:c.*255C>G	ENSP00000512595.1:n.*255C>G
ENST00000696386.1:c.220C>G	ENSP00000512596.1:p.Arg74Gly
ENST00000696387.1:c.*164C>G	ENSP00000512597.1:n.*164C>G
ENST00000696388.1:c.*383C>G	ENSP00000512598.1:n.*383C>G
ENST00000696389.1:c.*568C>G	ENSP00000512599.1:n.*568C>G
ENST00000696390.1:c.327C>G	ENSP00000512600.1:p.Gly109=
ENST00000696391.1:c.*393C>G	ENSP00000512601.1:n.*393C>G
ENST00000696392.1:c.537C>G	ENSP00000512602.1:p.Gly179=
ENST00000696393.1:c.537C>G	ENSP00000512603.1:p.Gly179=
ENST00000696405.1:c.537C>G	ENSP00000512607.1:p.Gly179=
ENST00000269097.9:c.537C>G MANE Select	ENSP00000269097.3:p.Gly179=
ENST00000269097.8:c.537C>G	ENSP00000269097.3:p.Gly179=
ENST00000585361.5:c.*374C>G	ENSP00000466983.1:n.*374C>G
ENST00000588558.5:c.*512C>G	ENSP00000467624.1:n.*512C>G
ENST00000590253.2:c.39C>G
ENST00000590639.1:n.558C>G
ENST00000591696.1:c.429C>G	ENSP00000468677.1:p.Gly143=
NM_138387.3:c.537C>G , LRG_182t1:c.537C>G	NP_612396.1:p.Gly179=
NR_028581.1:n.967C>G
NR_028582.1:n.832C>G
XM_006722179.2:c.418C>G	XP_006722242.1:p.Arg140Gly
XM_011525473.1:c.192C>G	XP_011523775.1:p.Gly64=
XM_011525474.1:c.192C>G	XP_011523776.1:p.Gly64=
NM_001319945.1:c.418C>G	NP_001306874.1:p.Arg140Gly
XM_011525473.3:c.192C>G	XP_011523775.1:p.Gly64=
XM_011525474.3:c.192C>G	XP_011523776.1:p.Gly64=
XM_017025335.2:c.192C>G	XP_016880824.1:p.Gly64=
NM_001319945.2:c.418C>G	NP_001306874.1:p.Arg140Gly
NR_028581.2:n.786C>G
NR_028582.2:n.651C>G
NM_001384165.1:c.192C>G	NP_001371094.1:p.Gly64=
NM_001384166.1:c.192C>G	NP_001371095.1:p.Gly64=
NM_001384167.1:c.192C>G	NP_001371096.1:p.Gly64=
NM_001384168.1:c.192C>G	NP_001371097.1:p.Gly64=
NM_138387.4:c.537C>G MANE Select	NP_612396.1:p.Gly179=