Canonical Allele Identifier: CA500617209

Gene: G6PC3

Linked Data

• gnomAD v4: 17-44075773-T-G
• MyVariant Identifiers: chr17:g.42153141T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075773T>G , CM000679.2:g.44075773T>G	GRCh38
NC_000017.10:g.42153141T>G , CM000679.1:g.42153141T>G	GRCh37
NC_000017.9:g.39508667T>G	NCBI36
NG_015818.1:g.10044T>G , LRG_182:g.10044T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*608T>G	ENSP00000466983.1:n.*608T>G
ENST00000588558.6:c.*746T>G	ENSP00000467624.1:n.*746T>G
ENST00000590253.3:c.*64T>G	ENSP00000465111.2:n.*64T>G
ENST00000593115.2:c.*792T>G	ENSP00000466821.1:n.*792T>G
ENST00000696383.1:c.426T>G	ENSP00000512593.1:p.Ala142=
ENST00000696384.1:c.*331T>G	ENSP00000512594.1:n.*331T>G
ENST00000696385.1:c.*489T>G	ENSP00000512595.1:n.*489T>G
ENST00000696386.1:c.*64T>G	ENSP00000512596.1:n.*64T>G
ENST00000696387.1:c.*398T>G	ENSP00000512597.1:n.*398T>G
ENST00000696388.1:c.*617T>G	ENSP00000512598.1:n.*617T>G
ENST00000696389.1:c.*802T>G	ENSP00000512599.1:n.*802T>G
ENST00000696390.1:c.561T>G	ENSP00000512600.1:p.Ala187=
ENST00000696391.1:c.*627T>G	ENSP00000512601.1:n.*627T>G
ENST00000696392.1:c.771T>G	ENSP00000512602.1:p.Ala257=
ENST00000696393.1:c.771T>G	ENSP00000512603.1:p.Ala257=
ENST00000696405.1:c.677+322T>G	ENSP00000512607.1:n.677+322T>G
ENST00000269097.9:c.771T>G MANE Select	ENSP00000269097.3:p.Ala257=
ENST00000269097.8:c.771T>G	ENSP00000269097.3:p.Ala257=
ENST00000585361.5:c.*608T>G	ENSP00000466983.1:n.*608T>G
ENST00000588558.5:c.*746T>G	ENSP00000467624.1:n.*746T>G
ENST00000590253.2:c.273T>G
ENST00000590639.1:n.792T>G
ENST00000591696.1:c.663T>G	ENSP00000468677.1:p.Ala221=
NM_138387.3:c.771T>G , LRG_182t1:c.771T>G	NP_612396.1:p.Ala257=
NR_028581.1:n.1201T>G
NR_028582.1:n.1066T>G
XM_011525473.1:c.426T>G	XP_011523775.1:p.Ala142=
XM_011525474.1:c.426T>G	XP_011523776.1:p.Ala142=
NM_001319945.1:c.*64T>G	NP_001306874.1:n.*64T>G
XM_011525473.3:c.426T>G	XP_011523775.1:p.Ala142=
XM_011525474.3:c.426T>G	XP_011523776.1:p.Ala142=
XM_017025335.2:c.426T>G	XP_016880824.1:p.Ala142=
NM_001319945.2:c.*64T>G	NP_001306874.1:n.*64T>G
NR_028581.2:n.1020T>G
NR_028582.2:n.885T>G
NM_001384165.1:c.426T>G	NP_001371094.1:p.Ala142=
NM_001384166.1:c.426T>G	NP_001371095.1:p.Ala142=
NM_001384167.1:c.426T>G	NP_001371096.1:p.Ala142=
NM_001384168.1:c.426T>G	NP_001371097.1:p.Ala142=
NM_138387.4:c.771T>G MANE Select	NP_612396.1:p.Ala257=