Canonical Allele Identifier: CA399727388

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42152696T>G (hg19) ; chr17:g.44075328T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075328T>G , CM000679.2:g.44075328T>G	GRCh38
NC_000017.10:g.42152696T>G , CM000679.1:g.42152696T>G	GRCh37
NC_000017.9:g.39508222T>G	NCBI36
NG_015818.1:g.9599T>G , LRG_182:g.9599T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000585361.6:c.*391T>G	ENSP00000466983.1:n.*391T>G
ENST00000588558.6:c.*529T>G	ENSP00000467624.1:n.*529T>G
ENST00000590253.3:c.435T>G	ENSP00000465111.2:p.Ala145=
ENST00000593115.2:c.*575T>G	ENSP00000466821.1:n.*575T>G
ENST00000696383.1:c.209T>G	ENSP00000512593.1:p.Leu70Arg
ENST00000696384.1:c.*114T>G	ENSP00000512594.1:n.*114T>G
ENST00000696385.1:c.*272T>G	ENSP00000512595.1:n.*272T>G
ENST00000696386.1:c.237T>G	ENSP00000512596.1:p.Ala79=
ENST00000696387.1:c.*181T>G	ENSP00000512597.1:n.*181T>G
ENST00000696388.1:c.*400T>G	ENSP00000512598.1:n.*400T>G
ENST00000696389.1:c.*585T>G	ENSP00000512599.1:n.*585T>G
ENST00000696390.1:c.344T>G	ENSP00000512600.1:p.Leu115Arg
ENST00000696391.1:c.*410T>G	ENSP00000512601.1:n.*410T>G
ENST00000696392.1:c.554T>G	ENSP00000512602.1:p.Leu185Arg
ENST00000696393.1:c.554T>G	ENSP00000512603.1:p.Leu185Arg
ENST00000696405.1:c.554T>G	ENSP00000512607.1:p.Leu185Arg
ENST00000269097.9:c.554T>G MANE Select	ENSP00000269097.3:p.Leu185Arg
ENST00000269097.8:c.554T>G	ENSP00000269097.3:p.Leu185Arg
ENST00000585361.5:c.*391T>G	ENSP00000466983.1:n.*391T>G
ENST00000588558.5:c.*529T>G	ENSP00000467624.1:n.*529T>G
ENST00000590253.2:c.56T>G
ENST00000590639.1:n.575T>G
ENST00000591696.1:c.446T>G	ENSP00000468677.1:p.Leu149Arg
NM_138387.3:c.554T>G , LRG_182t1:c.554T>G	NP_612396.1:p.Leu185Arg
NR_028581.1:n.984T>G
NR_028582.1:n.849T>G
XM_006722179.2:c.435T>G	XP_006722242.1:p.Ala145=
XM_011525473.1:c.209T>G	XP_011523775.1:p.Leu70Arg
XM_011525474.1:c.209T>G	XP_011523776.1:p.Leu70Arg
NM_001319945.1:c.435T>G	NP_001306874.1:p.Ala145=
XM_011525473.3:c.209T>G	XP_011523775.1:p.Leu70Arg
XM_011525474.3:c.209T>G	XP_011523776.1:p.Leu70Arg
XM_017025335.2:c.209T>G	XP_016880824.1:p.Leu70Arg
NM_001319945.2:c.435T>G	NP_001306874.1:p.Ala145=
NR_028581.2:n.803T>G
NR_028582.2:n.668T>G
NM_001384165.1:c.209T>G	NP_001371094.1:p.Leu70Arg
NM_001384166.1:c.209T>G	NP_001371095.1:p.Leu70Arg
NM_001384167.1:c.209T>G	NP_001371096.1:p.Leu70Arg
NM_001384168.1:c.209T>G	NP_001371097.1:p.Leu70Arg
NM_138387.4:c.554T>G MANE Select	NP_612396.1:p.Leu185Arg