Canonical Allele Identifier: CA399728806

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42152804G>C (hg19) ; chr17:g.44075436G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075436G>C , CM000679.2:g.44075436G>C	GRCh38
NC_000017.10:g.42152804G>C , CM000679.1:g.42152804G>C	GRCh37
NC_000017.9:g.39508330G>C	NCBI36
NG_015818.1:g.9707G>C , LRG_182:g.9707G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*499G>C	ENSP00000466983.1:n.*499G>C
ENST00000588558.6:c.*637G>C	ENSP00000467624.1:n.*637G>C
ENST00000590253.3:c.543G>C	ENSP00000465111.2:p.Gly181=
ENST00000593115.2:c.*683G>C	ENSP00000466821.1:n.*683G>C
ENST00000696383.1:c.317G>C	ENSP00000512593.1:p.Gly106Ala
ENST00000696384.1:c.*222G>C	ENSP00000512594.1:n.*222G>C
ENST00000696385.1:c.*380G>C	ENSP00000512595.1:n.*380G>C
ENST00000696386.1:c.345G>C	ENSP00000512596.1:p.Gly115=
ENST00000696387.1:c.*289G>C	ENSP00000512597.1:n.*289G>C
ENST00000696388.1:c.*508G>C	ENSP00000512598.1:n.*508G>C
ENST00000696389.1:c.*693G>C	ENSP00000512599.1:n.*693G>C
ENST00000696390.1:c.452G>C	ENSP00000512600.1:p.Gly151Ala
ENST00000696391.1:c.*518G>C	ENSP00000512601.1:n.*518G>C
ENST00000696392.1:c.662G>C	ENSP00000512602.1:p.Gly221Ala
ENST00000696393.1:c.662G>C	ENSP00000512603.1:p.Gly221Ala
ENST00000696405.1:c.662G>C	ENSP00000512607.1:p.Gly221Ala
ENST00000269097.9:c.662G>C MANE Select	ENSP00000269097.3:p.Gly221Ala
ENST00000269097.8:c.662G>C	ENSP00000269097.3:p.Gly221Ala
ENST00000585361.5:c.*499G>C	ENSP00000466983.1:n.*499G>C
ENST00000588558.5:c.*637G>C	ENSP00000467624.1:n.*637G>C
ENST00000590253.2:c.164G>C
ENST00000590639.1:n.683G>C
ENST00000591696.1:c.554G>C	ENSP00000468677.1:p.Gly185Ala
NM_138387.3:c.662G>C , LRG_182t1:c.662G>C	NP_612396.1:p.Gly221Ala
NR_028581.1:n.1092G>C
NR_028582.1:n.957G>C
XM_006722179.2:c.543G>C	XP_006722242.1:p.Gly181=
XM_011525473.1:c.317G>C	XP_011523775.1:p.Gly106Ala
XM_011525474.1:c.317G>C	XP_011523776.1:p.Gly106Ala
NM_001319945.1:c.543G>C	NP_001306874.1:p.Gly181=
XM_011525473.3:c.317G>C	XP_011523775.1:p.Gly106Ala
XM_011525474.3:c.317G>C	XP_011523776.1:p.Gly106Ala
XM_017025335.2:c.317G>C	XP_016880824.1:p.Gly106Ala
NM_001319945.2:c.543G>C	NP_001306874.1:p.Gly181=
NR_028581.2:n.911G>C
NR_028582.2:n.776G>C
NM_001384165.1:c.317G>C	NP_001371094.1:p.Gly106Ala
NM_001384166.1:c.317G>C	NP_001371095.1:p.Gly106Ala
NM_001384167.1:c.317G>C	NP_001371096.1:p.Gly106Ala
NM_001384168.1:c.317G>C	NP_001371097.1:p.Gly106Ala
NM_138387.4:c.662G>C MANE Select	NP_612396.1:p.Gly221Ala