Canonical Allele Identifier: CA2261216463

Gene: G6PC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075421C= , CM000679.2:g.44075421C=	GRCh38
NC_000017.10:g.42152789C= , CM000679.1:g.42152789C=	GRCh37
NC_000017.9:g.39508315C=	NCBI36
NG_015818.1:g.9692C= , LRG_182:g.9692C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*484C=	ENSP00000466983.1:n.*484C=
ENST00000588558.6:c.*622C=	ENSP00000467624.1:n.*622C=
ENST00000590253.3:c.528C=	ENSP00000465111.2:p.Asp176=
ENST00000593115.2:c.*668C=	ENSP00000466821.1:n.*668C=
ENST00000696383.1:c.302C=	ENSP00000512593.1:p.Thr101=
ENST00000696384.1:c.*207C=	ENSP00000512594.1:n.*207C=
ENST00000696385.1:c.*365C=	ENSP00000512595.1:n.*365C=
ENST00000696386.1:c.330C=	ENSP00000512596.1:p.Asp110=
ENST00000696387.1:c.*274C=	ENSP00000512597.1:n.*274C=
ENST00000696388.1:c.*493C=	ENSP00000512598.1:n.*493C=
ENST00000696389.1:c.*678C=	ENSP00000512599.1:n.*678C=
ENST00000696390.1:c.437C=	ENSP00000512600.1:p.Thr146=
ENST00000696391.1:c.*503C=	ENSP00000512601.1:n.*503C=
ENST00000696392.1:c.647C=	ENSP00000512602.1:p.Thr216=
ENST00000696393.1:c.647C=	ENSP00000512603.1:p.Thr216=
ENST00000696405.1:c.647C=	ENSP00000512607.1:p.Thr216=
ENST00000269097.9:c.647C= MANE Select	ENSP00000269097.3:p.Thr216=
ENST00000269097.8:c.647C=	ENSP00000269097.3:p.Thr216=
ENST00000585361.5:c.*484C=	ENSP00000466983.1:n.*484C=
ENST00000588558.5:c.*622C=	ENSP00000467624.1:n.*622C=
ENST00000590253.2:c.149C=
ENST00000590639.1:n.668C=
ENST00000591696.1:c.539C=	ENSP00000468677.1:p.Thr180=
NM_138387.3:c.647C= , LRG_182t1:c.647C=	NP_612396.1:p.Thr216=
NR_028581.1:n.1077C=
NR_028582.1:n.942C=
XM_006722179.2:c.528C=	XP_006722242.1:p.Asp176=
XM_011525473.1:c.302C=	XP_011523775.1:p.Thr101=
XM_011525474.1:c.302C=	XP_011523776.1:p.Thr101=
NM_001319945.1:c.528C=	NP_001306874.1:p.Asp176=
XM_011525473.3:c.302C=	XP_011523775.1:p.Thr101=
XM_011525474.3:c.302C=	XP_011523776.1:p.Thr101=
XM_017025335.2:c.302C=	XP_016880824.1:p.Thr101=
NM_001319945.2:c.528C=	NP_001306874.1:p.Asp176=
NR_028581.2:n.896C=
NR_028582.2:n.761C=
NM_001384165.1:c.302C=	NP_001371094.1:p.Thr101=
NM_001384166.1:c.302C=	NP_001371095.1:p.Thr101=
NM_001384167.1:c.302C=	NP_001371096.1:p.Thr101=
NM_001384168.1:c.302C=	NP_001371097.1:p.Thr101=
NM_138387.4:c.647C= MANE Select	NP_612396.1:p.Thr216=