Canonical Allele Identifier: CA2261216437
Gene: G6PC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44075354C= , CM000679.2:g.44075354C= GRCh38
NC_000017.10:g.42152722C= , CM000679.1:g.42152722C= GRCh37
NC_000017.9:g.39508248C= NCBI36
NG_015818.1:g.9625C= , LRG_182:g.9625C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585361.6:c.*417C= ENSP00000466983.1:n.*417C=
ENST00000588558.6:c.*555C= ENSP00000467624.1:n.*555C=
ENST00000590253.3:c.461C= ENSP00000465111.2:p.Ala154=
ENST00000593115.2:c.*601C= ENSP00000466821.1:n.*601C=
ENST00000696383.1:c.235C= ENSP00000512593.1:p.Arg79=
ENST00000696384.1:c.*140C= ENSP00000512594.1:n.*140C=
ENST00000696385.1:c.*298C= ENSP00000512595.1:n.*298C=
ENST00000696386.1:c.263C= ENSP00000512596.1:p.Ala88=
ENST00000696387.1:c.*207C= ENSP00000512597.1:n.*207C=
ENST00000696388.1:c.*426C= ENSP00000512598.1:n.*426C=
ENST00000696389.1:c.*611C= ENSP00000512599.1:n.*611C=
ENST00000696390.1:c.370C= ENSP00000512600.1:p.Arg124=
ENST00000696391.1:c.*436C= ENSP00000512601.1:n.*436C=
ENST00000696392.1:c.580C= ENSP00000512602.1:p.Arg194=
ENST00000696393.1:c.580C= ENSP00000512603.1:p.Arg194=
ENST00000696405.1:c.580C= ENSP00000512607.1:p.Arg194=
ENST00000269097.9:c.580C= MANE Select ENSP00000269097.3:p.Arg194=
ENST00000269097.8:c.580C= ENSP00000269097.3:p.Arg194=
ENST00000585361.5:c.*417C= ENSP00000466983.1:n.*417C=
ENST00000588558.5:c.*555C= ENSP00000467624.1:n.*555C=
ENST00000590253.2:c.82C=
ENST00000590639.1:n.601C=
ENST00000591696.1:c.472C= ENSP00000468677.1:p.Arg158=
NM_138387.3:c.580C= , LRG_182t1:c.580C= NP_612396.1:p.Arg194=
NR_028581.1:n.1010C=
NR_028582.1:n.875C=
XM_006722179.2:c.461C= XP_006722242.1:p.Ala154=
XM_011525473.1:c.235C= XP_011523775.1:p.Arg79=
XM_011525474.1:c.235C= XP_011523776.1:p.Arg79=
NM_001319945.1:c.461C= NP_001306874.1:p.Ala154=
XM_011525473.3:c.235C= XP_011523775.1:p.Arg79=
XM_011525474.3:c.235C= XP_011523776.1:p.Arg79=
XM_017025335.2:c.235C= XP_016880824.1:p.Arg79=
NM_001319945.2:c.461C= NP_001306874.1:p.Ala154=
NR_028581.2:n.829C=
NR_028582.2:n.694C=
NM_001384165.1:c.235C= NP_001371094.1:p.Arg79=
NM_001384166.1:c.235C= NP_001371095.1:p.Arg79=
NM_001384167.1:c.235C= NP_001371096.1:p.Arg79=
NM_001384168.1:c.235C= NP_001371097.1:p.Arg79=
NM_138387.4:c.580C= MANE Select NP_612396.1:p.Arg194=