Canonical Allele Identifier: CA500617039

Gene: G6PC3

Linked Data

• gnomAD v4: 17-44075695-C-T
• MyVariant Identifiers: chr17:g.42153063C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075695C>T , CM000679.2:g.44075695C>T	GRCh38
NC_000017.10:g.42153063C>T , CM000679.1:g.42153063C>T	GRCh37
NC_000017.9:g.39508589C>T	NCBI36
NG_015818.1:g.9966C>T , LRG_182:g.9966C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585361.6:c.*530C>T	ENSP00000466983.1:n.*530C>T
ENST00000588558.6:c.*668C>T	ENSP00000467624.1:n.*668C>T
ENST00000590253.3:c.574C>T	ENSP00000465111.2:p.Leu192Phe
ENST00000593115.2:c.*714C>T	ENSP00000466821.1:n.*714C>T
ENST00000696383.1:c.348C>T	ENSP00000512593.1:p.Ala116=
ENST00000696384.1:c.*253C>T	ENSP00000512594.1:n.*253C>T
ENST00000696385.1:c.*411C>T	ENSP00000512595.1:n.*411C>T
ENST00000696386.1:c.376C>T	ENSP00000512596.1:p.Leu126Phe
ENST00000696387.1:c.*320C>T	ENSP00000512597.1:n.*320C>T
ENST00000696388.1:c.*539C>T	ENSP00000512598.1:n.*539C>T
ENST00000696389.1:c.*724C>T	ENSP00000512599.1:n.*724C>T
ENST00000696390.1:c.483C>T	ENSP00000512600.1:p.Ala161=
ENST00000696391.1:c.*549C>T	ENSP00000512601.1:n.*549C>T
ENST00000696392.1:c.693C>T	ENSP00000512602.1:p.Ala231=
ENST00000696393.1:c.693C>T	ENSP00000512603.1:p.Ala231=
ENST00000696405.1:c.677+244C>T	ENSP00000512607.1:n.677+244C>T
ENST00000269097.9:c.693C>T MANE Select	ENSP00000269097.3:p.Ala231=
ENST00000269097.8:c.693C>T	ENSP00000269097.3:p.Ala231=
ENST00000585361.5:c.*530C>T	ENSP00000466983.1:n.*530C>T
ENST00000588558.5:c.*668C>T	ENSP00000467624.1:n.*668C>T
ENST00000590253.2:c.195C>T
ENST00000590639.1:n.714C>T
ENST00000591696.1:c.585C>T	ENSP00000468677.1:p.Ala195=
NM_138387.3:c.693C>T , LRG_182t1:c.693C>T	NP_612396.1:p.Ala231=
NR_028581.1:n.1123C>T
NR_028582.1:n.988C>T
XM_006722179.2:c.574C>T	XP_006722242.1:p.Leu192Phe
XM_011525473.1:c.348C>T	XP_011523775.1:p.Ala116=
XM_011525474.1:c.348C>T	XP_011523776.1:p.Ala116=
NM_001319945.1:c.574C>T	NP_001306874.1:p.Leu192Phe
XM_011525473.3:c.348C>T	XP_011523775.1:p.Ala116=
XM_011525474.3:c.348C>T	XP_011523776.1:p.Ala116=
XM_017025335.2:c.348C>T	XP_016880824.1:p.Ala116=
NM_001319945.2:c.574C>T	NP_001306874.1:p.Leu192Phe
NR_028581.2:n.942C>T
NR_028582.2:n.807C>T
NM_001384165.1:c.348C>T	NP_001371094.1:p.Ala116=
NM_001384166.1:c.348C>T	NP_001371095.1:p.Ala116=
NM_001384167.1:c.348C>T	NP_001371096.1:p.Ala116=
NM_001384168.1:c.348C>T	NP_001371097.1:p.Ala116=
NM_138387.4:c.693C>T MANE Select	NP_612396.1:p.Ala231=