Canonical Allele Identifier: CA500617226

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42153156C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075788C>T , CM000679.2:g.44075788C>T	GRCh38
NC_000017.10:g.42153156C>T , CM000679.1:g.42153156C>T	GRCh37
NC_000017.9:g.39508682C>T	NCBI36
NG_015818.1:g.10059C>T , LRG_182:g.10059C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585361.6:c.*623C>T	ENSP00000466983.1:n.*623C>T
ENST00000588558.6:c.*761C>T	ENSP00000467624.1:n.*761C>T
ENST00000590253.3:c.*79C>T	ENSP00000465111.2:n.*79C>T
ENST00000593115.2:c.*807C>T	ENSP00000466821.1:n.*807C>T
ENST00000696383.1:c.441C>T	ENSP00000512593.1:p.Gly147=
ENST00000696384.1:c.*346C>T	ENSP00000512594.1:n.*346C>T
ENST00000696385.1:c.*504C>T	ENSP00000512595.1:n.*504C>T
ENST00000696386.1:c.*79C>T	ENSP00000512596.1:n.*79C>T
ENST00000696387.1:c.*413C>T	ENSP00000512597.1:n.*413C>T
ENST00000696388.1:c.*632C>T	ENSP00000512598.1:n.*632C>T
ENST00000696389.1:c.*817C>T	ENSP00000512599.1:n.*817C>T
ENST00000696390.1:c.576C>T	ENSP00000512600.1:p.Gly192=
ENST00000696391.1:c.*642C>T	ENSP00000512601.1:n.*642C>T
ENST00000696392.1:c.786C>T	ENSP00000512602.1:p.Gly262=
ENST00000696393.1:c.786C>T	ENSP00000512603.1:p.Gly262=
ENST00000696405.1:c.677+337C>T	ENSP00000512607.1:n.677+337C>T
ENST00000269097.9:c.786C>T MANE Select	ENSP00000269097.3:p.Gly262=
ENST00000269097.8:c.786C>T	ENSP00000269097.3:p.Gly262=
ENST00000585361.5:c.*623C>T	ENSP00000466983.1:n.*623C>T
ENST00000588558.5:c.*761C>T	ENSP00000467624.1:n.*761C>T
ENST00000590253.2:c.288C>T
ENST00000590639.1:n.807C>T
ENST00000591696.1:c.678C>T	ENSP00000468677.1:p.Gly226=
NM_138387.3:c.786C>T , LRG_182t1:c.786C>T	NP_612396.1:p.Gly262=
NR_028581.1:n.1216C>T
NR_028582.1:n.1081C>T
XM_011525473.1:c.441C>T	XP_011523775.1:p.Gly147=
XM_011525474.1:c.441C>T	XP_011523776.1:p.Gly147=
NM_001319945.1:c.*79C>T	NP_001306874.1:n.*79C>T
XM_011525473.3:c.441C>T	XP_011523775.1:p.Gly147=
XM_011525474.3:c.441C>T	XP_011523776.1:p.Gly147=
XM_017025335.2:c.441C>T	XP_016880824.1:p.Gly147=
NM_001319945.2:c.*79C>T	NP_001306874.1:n.*79C>T
NR_028581.2:n.1035C>T
NR_028582.2:n.900C>T
NM_001384165.1:c.441C>T	NP_001371094.1:p.Gly147=
NM_001384166.1:c.441C>T	NP_001371095.1:p.Gly147=
NM_001384167.1:c.441C>T	NP_001371096.1:p.Gly147=
NM_001384168.1:c.441C>T	NP_001371097.1:p.Gly147=
NM_138387.4:c.786C>T MANE Select	NP_612396.1:p.Gly262=