Canonical Allele Identifier: CA399729158

Gene: G6PC3

Linked Data

• gnomAD v4: 17-44075710-G-T
• MyVariant Identifiers: chr17:g.42153078G>T (hg19) ; chr17:g.44075710G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075710G>T , CM000679.2:g.44075710G>T	GRCh38
NC_000017.10:g.42153078G>T , CM000679.1:g.42153078G>T	GRCh37
NC_000017.9:g.39508604G>T	NCBI36
NG_015818.1:g.9981G>T , LRG_182:g.9981G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*545G>T	ENSP00000466983.1:n.*545G>T
ENST00000588558.6:c.*683G>T	ENSP00000467624.1:n.*683G>T
ENST00000590253.3:c.*1G>T	ENSP00000465111.2:n.*1G>T
ENST00000593115.2:c.*729G>T	ENSP00000466821.1:n.*729G>T
ENST00000696383.1:c.363G>T	ENSP00000512593.1:p.Glu121Asp
ENST00000696384.1:c.*268G>T	ENSP00000512594.1:n.*268G>T
ENST00000696385.1:c.*426G>T	ENSP00000512595.1:n.*426G>T
ENST00000696386.1:c.*1G>T	ENSP00000512596.1:n.*1G>T
ENST00000696387.1:c.*335G>T	ENSP00000512597.1:n.*335G>T
ENST00000696388.1:c.*554G>T	ENSP00000512598.1:n.*554G>T
ENST00000696389.1:c.*739G>T	ENSP00000512599.1:n.*739G>T
ENST00000696390.1:c.498G>T	ENSP00000512600.1:p.Glu166Asp
ENST00000696391.1:c.*564G>T	ENSP00000512601.1:n.*564G>T
ENST00000696392.1:c.708G>T	ENSP00000512602.1:p.Glu236Asp
ENST00000696393.1:c.708G>T	ENSP00000512603.1:p.Glu236Asp
ENST00000696405.1:c.677+259G>T	ENSP00000512607.1:n.677+259G>T
ENST00000269097.9:c.708G>T MANE Select	ENSP00000269097.3:p.Glu236Asp
ENST00000269097.8:c.708G>T	ENSP00000269097.3:p.Glu236Asp
ENST00000585361.5:c.*545G>T	ENSP00000466983.1:n.*545G>T
ENST00000588558.5:c.*683G>T	ENSP00000467624.1:n.*683G>T
ENST00000590253.2:c.210G>T
ENST00000590639.1:n.729G>T
ENST00000591696.1:c.600G>T	ENSP00000468677.1:p.Glu200Asp
NM_138387.3:c.708G>T , LRG_182t1:c.708G>T	NP_612396.1:p.Glu236Asp
NR_028581.1:n.1138G>T
NR_028582.1:n.1003G>T
XM_006722179.2:c.*1G>T	XP_006722242.1:n.*1G>T
XM_011525473.1:c.363G>T	XP_011523775.1:p.Glu121Asp
XM_011525474.1:c.363G>T	XP_011523776.1:p.Glu121Asp
NM_001319945.1:c.*1G>T	NP_001306874.1:n.*1G>T
XM_011525473.3:c.363G>T	XP_011523775.1:p.Glu121Asp
XM_011525474.3:c.363G>T	XP_011523776.1:p.Glu121Asp
XM_017025335.2:c.363G>T	XP_016880824.1:p.Glu121Asp
NM_001319945.2:c.*1G>T	NP_001306874.1:n.*1G>T
NR_028581.2:n.957G>T
NR_028582.2:n.822G>T
NM_001384165.1:c.363G>T	NP_001371094.1:p.Glu121Asp
NM_001384166.1:c.363G>T	NP_001371095.1:p.Glu121Asp
NM_001384167.1:c.363G>T	NP_001371096.1:p.Glu121Asp
NM_001384168.1:c.363G>T	NP_001371097.1:p.Glu121Asp
NM_138387.4:c.708G>T MANE Select	NP_612396.1:p.Glu236Asp