Canonical Allele Identifier: CA2261216434

Gene: G6PC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075347T= , CM000679.2:g.44075347T=	GRCh38
NC_000017.10:g.42152715T= , CM000679.1:g.42152715T=	GRCh37
NC_000017.9:g.39508241T=	NCBI36
NG_015818.1:g.9618T= , LRG_182:g.9618T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*410T=	ENSP00000466983.1:n.*410T=
ENST00000588558.6:c.*548T=	ENSP00000467624.1:n.*548T=
ENST00000590253.3:c.454T=	ENSP00000465111.2:p.Tyr152=
ENST00000593115.2:c.*594T=	ENSP00000466821.1:n.*594T=
ENST00000696383.1:c.228T=	ENSP00000512593.1:p.Pro76=
ENST00000696384.1:c.*133T=	ENSP00000512594.1:n.*133T=
ENST00000696385.1:c.*291T=	ENSP00000512595.1:n.*291T=
ENST00000696386.1:c.256T=	ENSP00000512596.1:p.Tyr86=
ENST00000696387.1:c.*200T=	ENSP00000512597.1:n.*200T=
ENST00000696388.1:c.*419T=	ENSP00000512598.1:n.*419T=
ENST00000696389.1:c.*604T=	ENSP00000512599.1:n.*604T=
ENST00000696390.1:c.363T=	ENSP00000512600.1:p.Pro121=
ENST00000696391.1:c.*429T=	ENSP00000512601.1:n.*429T=
ENST00000696392.1:c.573T=	ENSP00000512602.1:p.Pro191=
ENST00000696393.1:c.573T=	ENSP00000512603.1:p.Pro191=
ENST00000696405.1:c.573T=	ENSP00000512607.1:p.Pro191=
ENST00000269097.9:c.573T= MANE Select	ENSP00000269097.3:p.Pro191=
ENST00000269097.8:c.573T=	ENSP00000269097.3:p.Pro191=
ENST00000585361.5:c.*410T=	ENSP00000466983.1:n.*410T=
ENST00000588558.5:c.*548T=	ENSP00000467624.1:n.*548T=
ENST00000590253.2:c.75T=
ENST00000590639.1:n.594T=
ENST00000591696.1:c.465T=	ENSP00000468677.1:p.Pro155=
NM_138387.3:c.573T= , LRG_182t1:c.573T=	NP_612396.1:p.Pro191=
NR_028581.1:n.1003T=
NR_028582.1:n.868T=
XM_006722179.2:c.454T=	XP_006722242.1:p.Tyr152=
XM_011525473.1:c.228T=	XP_011523775.1:p.Pro76=
XM_011525474.1:c.228T=	XP_011523776.1:p.Pro76=
NM_001319945.1:c.454T=	NP_001306874.1:p.Tyr152=
XM_011525473.3:c.228T=	XP_011523775.1:p.Pro76=
XM_011525474.3:c.228T=	XP_011523776.1:p.Pro76=
XM_017025335.2:c.228T=	XP_016880824.1:p.Pro76=
NM_001319945.2:c.454T=	NP_001306874.1:p.Tyr152=
NR_028581.2:n.822T=
NR_028582.2:n.687T=
NM_001384165.1:c.228T=	NP_001371094.1:p.Pro76=
NM_001384166.1:c.228T=	NP_001371095.1:p.Pro76=
NM_001384167.1:c.228T=	NP_001371096.1:p.Pro76=
NM_001384168.1:c.228T=	NP_001371097.1:p.Pro76=
NM_138387.4:c.573T= MANE Select	NP_612396.1:p.Pro191=