Canonical Allele Identifier: CA500616898

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42152751A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075383A>T , CM000679.2:g.44075383A>T	GRCh38
NC_000017.10:g.42152751A>T , CM000679.1:g.42152751A>T	GRCh37
NC_000017.9:g.39508277A>T	NCBI36
NG_015818.1:g.9654A>T , LRG_182:g.9654A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*446A>T	ENSP00000466983.1:n.*446A>T
ENST00000588558.6:c.*584A>T	ENSP00000467624.1:n.*584A>T
ENST00000590253.3:c.490A>T	ENSP00000465111.2:p.Thr164Ser
ENST00000593115.2:c.*630A>T	ENSP00000466821.1:n.*630A>T
ENST00000696383.1:c.264A>T	ENSP00000512593.1:p.Ala88=
ENST00000696384.1:c.*169A>T	ENSP00000512594.1:n.*169A>T
ENST00000696385.1:c.*327A>T	ENSP00000512595.1:n.*327A>T
ENST00000696386.1:c.292A>T	ENSP00000512596.1:p.Thr98Ser
ENST00000696387.1:c.*236A>T	ENSP00000512597.1:n.*236A>T
ENST00000696388.1:c.*455A>T	ENSP00000512598.1:n.*455A>T
ENST00000696389.1:c.*640A>T	ENSP00000512599.1:n.*640A>T
ENST00000696390.1:c.399A>T	ENSP00000512600.1:p.Ala133=
ENST00000696391.1:c.*465A>T	ENSP00000512601.1:n.*465A>T
ENST00000696392.1:c.609A>T	ENSP00000512602.1:p.Ala203=
ENST00000696393.1:c.609A>T	ENSP00000512603.1:p.Ala203=
ENST00000696405.1:c.609A>T	ENSP00000512607.1:p.Ala203=
ENST00000269097.9:c.609A>T MANE Select	ENSP00000269097.3:p.Ala203=
ENST00000269097.8:c.609A>T	ENSP00000269097.3:p.Ala203=
ENST00000585361.5:c.*446A>T	ENSP00000466983.1:n.*446A>T
ENST00000588558.5:c.*584A>T	ENSP00000467624.1:n.*584A>T
ENST00000590253.2:c.111A>T
ENST00000590639.1:n.630A>T
ENST00000591696.1:c.501A>T	ENSP00000468677.1:p.Ala167=
NM_138387.3:c.609A>T , LRG_182t1:c.609A>T	NP_612396.1:p.Ala203=
NR_028581.1:n.1039A>T
NR_028582.1:n.904A>T
XM_006722179.2:c.490A>T	XP_006722242.1:p.Thr164Ser
XM_011525473.1:c.264A>T	XP_011523775.1:p.Ala88=
XM_011525474.1:c.264A>T	XP_011523776.1:p.Ala88=
NM_001319945.1:c.490A>T	NP_001306874.1:p.Thr164Ser
XM_011525473.3:c.264A>T	XP_011523775.1:p.Ala88=
XM_011525474.3:c.264A>T	XP_011523776.1:p.Ala88=
XM_017025335.2:c.264A>T	XP_016880824.1:p.Ala88=
NM_001319945.2:c.490A>T	NP_001306874.1:p.Thr164Ser
NR_028581.2:n.858A>T
NR_028582.2:n.723A>T
NM_001384165.1:c.264A>T	NP_001371094.1:p.Ala88=
NM_001384166.1:c.264A>T	NP_001371095.1:p.Ala88=
NM_001384167.1:c.264A>T	NP_001371096.1:p.Ala88=
NM_001384168.1:c.264A>T	NP_001371097.1:p.Ala88=
NM_138387.4:c.609A>T MANE Select	NP_612396.1:p.Ala203=