Canonical Allele Identifier: CA2261216415

Gene: G6PC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075313C= , CM000679.2:g.44075313C=	GRCh38
NC_000017.10:g.42152681C= , CM000679.1:g.42152681C=	GRCh37
NC_000017.9:g.39508207C=	NCBI36
NG_015818.1:g.9584C= , LRG_182:g.9584C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*376C=	ENSP00000466983.1:n.*376C=
ENST00000588558.6:c.*514C=	ENSP00000467624.1:n.*514C=
ENST00000590253.3:c.420C=	ENSP00000465111.2:p.Arg140=
ENST00000593115.2:c.*560C=	ENSP00000466821.1:n.*560C=
ENST00000696383.1:c.194C=	ENSP00000512593.1:p.Ala65=
ENST00000696384.1:c.*99C=	ENSP00000512594.1:n.*99C=
ENST00000696385.1:c.*257C=	ENSP00000512595.1:n.*257C=
ENST00000696386.1:c.222C=	ENSP00000512596.1:p.Arg74=
ENST00000696387.1:c.*166C=	ENSP00000512597.1:n.*166C=
ENST00000696388.1:c.*385C=	ENSP00000512598.1:n.*385C=
ENST00000696389.1:c.*570C=	ENSP00000512599.1:n.*570C=
ENST00000696390.1:c.329C=	ENSP00000512600.1:p.Ala110=
ENST00000696391.1:c.*395C=	ENSP00000512601.1:n.*395C=
ENST00000696392.1:c.539C=	ENSP00000512602.1:p.Ala180=
ENST00000696393.1:c.539C=	ENSP00000512603.1:p.Ala180=
ENST00000696405.1:c.539C=	ENSP00000512607.1:p.Ala180=
ENST00000269097.9:c.539C= MANE Select	ENSP00000269097.3:p.Ala180=
ENST00000269097.8:c.539C=	ENSP00000269097.3:p.Ala180=
ENST00000585361.5:c.*376C=	ENSP00000466983.1:n.*376C=
ENST00000588558.5:c.*514C=	ENSP00000467624.1:n.*514C=
ENST00000590253.2:c.41C=
ENST00000590639.1:n.560C=
ENST00000591696.1:c.431C=	ENSP00000468677.1:p.Ala144=
NM_138387.3:c.539C= , LRG_182t1:c.539C=	NP_612396.1:p.Ala180=
NR_028581.1:n.969C=
NR_028582.1:n.834C=
XM_006722179.2:c.420C=	XP_006722242.1:p.Arg140=
XM_011525473.1:c.194C=	XP_011523775.1:p.Ala65=
XM_011525474.1:c.194C=	XP_011523776.1:p.Ala65=
NM_001319945.1:c.420C=	NP_001306874.1:p.Arg140=
XM_011525473.3:c.194C=	XP_011523775.1:p.Ala65=
XM_011525474.3:c.194C=	XP_011523776.1:p.Ala65=
XM_017025335.2:c.194C=	XP_016880824.1:p.Ala65=
NM_001319945.2:c.420C=	NP_001306874.1:p.Arg140=
NR_028581.2:n.788C=
NR_028582.2:n.653C=
NM_001384165.1:c.194C=	NP_001371094.1:p.Ala65=
NM_001384166.1:c.194C=	NP_001371095.1:p.Ala65=
NM_001384167.1:c.194C=	NP_001371096.1:p.Ala65=
NM_001384168.1:c.194C=	NP_001371097.1:p.Ala65=
NM_138387.4:c.539C= MANE Select	NP_612396.1:p.Ala180=