Canonical Allele Identifier: CA399729272

Gene: G6PC3

Linked Data

• MyVariant Identifiers: chr17:g.42153132C>A (hg19) ; chr17:g.44075764C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075764C>A , CM000679.2:g.44075764C>A	GRCh38
NC_000017.10:g.42153132C>A , CM000679.1:g.42153132C>A	GRCh37
NC_000017.9:g.39508658C>A	NCBI36
NG_015818.1:g.10035C>A , LRG_182:g.10035C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*599C>A	ENSP00000466983.1:n.*599C>A
ENST00000588558.6:c.*737C>A	ENSP00000467624.1:n.*737C>A
ENST00000590253.3:c.*55C>A	ENSP00000465111.2:n.*55C>A
ENST00000593115.2:c.*783C>A	ENSP00000466821.1:n.*783C>A
ENST00000696383.1:c.417C>A	ENSP00000512593.1:p.Asp139Glu
ENST00000696384.1:c.*322C>A	ENSP00000512594.1:n.*322C>A
ENST00000696385.1:c.*480C>A	ENSP00000512595.1:n.*480C>A
ENST00000696386.1:c.*55C>A	ENSP00000512596.1:n.*55C>A
ENST00000696387.1:c.*389C>A	ENSP00000512597.1:n.*389C>A
ENST00000696388.1:c.*608C>A	ENSP00000512598.1:n.*608C>A
ENST00000696389.1:c.*793C>A	ENSP00000512599.1:n.*793C>A
ENST00000696390.1:c.552C>A	ENSP00000512600.1:p.Asp184Glu
ENST00000696391.1:c.*618C>A	ENSP00000512601.1:n.*618C>A
ENST00000696392.1:c.762C>A	ENSP00000512602.1:p.Asp254Glu
ENST00000696393.1:c.762C>A	ENSP00000512603.1:p.Asp254Glu
ENST00000696405.1:c.677+313C>A	ENSP00000512607.1:n.677+313C>A
ENST00000269097.9:c.762C>A MANE Select	ENSP00000269097.3:p.Asp254Glu
ENST00000269097.8:c.762C>A	ENSP00000269097.3:p.Asp254Glu
ENST00000585361.5:c.*599C>A	ENSP00000466983.1:n.*599C>A
ENST00000588558.5:c.*737C>A	ENSP00000467624.1:n.*737C>A
ENST00000590253.2:c.264C>A
ENST00000590639.1:n.783C>A
ENST00000591696.1:c.654C>A	ENSP00000468677.1:p.Asp218Glu
NM_138387.3:c.762C>A , LRG_182t1:c.762C>A	NP_612396.1:p.Asp254Glu
NR_028581.1:n.1192C>A
NR_028582.1:n.1057C>A
XM_011525473.1:c.417C>A	XP_011523775.1:p.Asp139Glu
XM_011525474.1:c.417C>A	XP_011523776.1:p.Asp139Glu
NM_001319945.1:c.*55C>A	NP_001306874.1:n.*55C>A
XM_011525473.3:c.417C>A	XP_011523775.1:p.Asp139Glu
XM_011525474.3:c.417C>A	XP_011523776.1:p.Asp139Glu
XM_017025335.2:c.417C>A	XP_016880824.1:p.Asp139Glu
NM_001319945.2:c.*55C>A	NP_001306874.1:n.*55C>A
NR_028581.2:n.1011C>A
NR_028582.2:n.876C>A
NM_001384165.1:c.417C>A	NP_001371094.1:p.Asp139Glu
NM_001384166.1:c.417C>A	NP_001371095.1:p.Asp139Glu
NM_001384167.1:c.417C>A	NP_001371096.1:p.Asp139Glu
NM_001384168.1:c.417C>A	NP_001371097.1:p.Asp139Glu
NM_138387.4:c.762C>A MANE Select	NP_612396.1:p.Asp254Glu