Canonical Allele Identifier: CA399727398

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42152698A>G (hg19) ; chr17:g.44075330A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075330A>G , CM000679.2:g.44075330A>G	GRCh38
NC_000017.10:g.42152698A>G , CM000679.1:g.42152698A>G	GRCh37
NC_000017.9:g.39508224A>G	NCBI36
NG_015818.1:g.9601A>G , LRG_182:g.9601A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585361.6:c.*393A>G	ENSP00000466983.1:n.*393A>G
ENST00000588558.6:c.*531A>G	ENSP00000467624.1:n.*531A>G
ENST00000590253.3:c.437A>G	ENSP00000465111.2:p.Asp146Gly
ENST00000593115.2:c.*577A>G	ENSP00000466821.1:n.*577A>G
ENST00000696383.1:c.211A>G	ENSP00000512593.1:p.Met71Val
ENST00000696384.1:c.*116A>G	ENSP00000512594.1:n.*116A>G
ENST00000696385.1:c.*274A>G	ENSP00000512595.1:n.*274A>G
ENST00000696386.1:c.239A>G	ENSP00000512596.1:p.Asp80Gly
ENST00000696387.1:c.*183A>G	ENSP00000512597.1:n.*183A>G
ENST00000696388.1:c.*402A>G	ENSP00000512598.1:n.*402A>G
ENST00000696389.1:c.*587A>G	ENSP00000512599.1:n.*587A>G
ENST00000696390.1:c.346A>G	ENSP00000512600.1:p.Met116Val
ENST00000696391.1:c.*412A>G	ENSP00000512601.1:n.*412A>G
ENST00000696392.1:c.556A>G	ENSP00000512602.1:p.Met186Val
ENST00000696393.1:c.556A>G	ENSP00000512603.1:p.Met186Val
ENST00000696405.1:c.556A>G	ENSP00000512607.1:p.Met186Val
ENST00000269097.9:c.556A>G MANE Select	ENSP00000269097.3:p.Met186Val
ENST00000269097.8:c.556A>G	ENSP00000269097.3:p.Met186Val
ENST00000585361.5:c.*393A>G	ENSP00000466983.1:n.*393A>G
ENST00000588558.5:c.*531A>G	ENSP00000467624.1:n.*531A>G
ENST00000590253.2:c.58A>G
ENST00000590639.1:n.577A>G
ENST00000591696.1:c.448A>G	ENSP00000468677.1:p.Met150Val
NM_138387.3:c.556A>G , LRG_182t1:c.556A>G	NP_612396.1:p.Met186Val
NR_028581.1:n.986A>G
NR_028582.1:n.851A>G
XM_006722179.2:c.437A>G	XP_006722242.1:p.Asp146Gly
XM_011525473.1:c.211A>G	XP_011523775.1:p.Met71Val
XM_011525474.1:c.211A>G	XP_011523776.1:p.Met71Val
NM_001319945.1:c.437A>G	NP_001306874.1:p.Asp146Gly
XM_011525473.3:c.211A>G	XP_011523775.1:p.Met71Val
XM_011525474.3:c.211A>G	XP_011523776.1:p.Met71Val
XM_017025335.2:c.211A>G	XP_016880824.1:p.Met71Val
NM_001319945.2:c.437A>G	NP_001306874.1:p.Asp146Gly
NR_028581.2:n.805A>G
NR_028582.2:n.670A>G
NM_001384165.1:c.211A>G	NP_001371094.1:p.Met71Val
NM_001384166.1:c.211A>G	NP_001371095.1:p.Met71Val
NM_001384167.1:c.211A>G	NP_001371096.1:p.Met71Val
NM_001384168.1:c.211A>G	NP_001371097.1:p.Met71Val
NM_138387.4:c.556A>G MANE Select	NP_612396.1:p.Met186Val