Canonical Allele Identifier: CA2261216645
Gene: G6PC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44075738C= , CM000679.2:g.44075738C= GRCh38
NC_000017.10:g.42153106C= , CM000679.1:g.42153106C= GRCh37
NC_000017.9:g.39508632C= NCBI36
NG_015818.1:g.10009C= , LRG_182:g.10009C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585361.6:c.*573C= ENSP00000466983.1:n.*573C=
ENST00000588558.6:c.*711C= ENSP00000467624.1:n.*711C=
ENST00000590253.3:c.*29C= ENSP00000465111.2:n.*29C=
ENST00000593115.2:c.*757C= ENSP00000466821.1:n.*757C=
ENST00000696383.1:c.391C= ENSP00000512593.1:p.Arg131=
ENST00000696384.1:c.*296C= ENSP00000512594.1:n.*296C=
ENST00000696385.1:c.*454C= ENSP00000512595.1:n.*454C=
ENST00000696386.1:c.*29C= ENSP00000512596.1:n.*29C=
ENST00000696387.1:c.*363C= ENSP00000512597.1:n.*363C=
ENST00000696388.1:c.*582C= ENSP00000512598.1:n.*582C=
ENST00000696389.1:c.*767C= ENSP00000512599.1:n.*767C=
ENST00000696390.1:c.526C= ENSP00000512600.1:p.Arg176=
ENST00000696391.1:c.*592C= ENSP00000512601.1:n.*592C=
ENST00000696392.1:c.736C= ENSP00000512602.1:p.Arg246=
ENST00000696393.1:c.736C= ENSP00000512603.1:p.Arg246=
ENST00000696405.1:c.677+287C= ENSP00000512607.1:n.677+287C=
ENST00000269097.9:c.736C= MANE Select ENSP00000269097.3:p.Arg246=
ENST00000269097.8:c.736C= ENSP00000269097.3:p.Arg246=
ENST00000585361.5:c.*573C= ENSP00000466983.1:n.*573C=
ENST00000588558.5:c.*711C= ENSP00000467624.1:n.*711C=
ENST00000590253.2:c.238C=
ENST00000590639.1:n.757C=
ENST00000591696.1:c.628C= ENSP00000468677.1:p.Arg210=
NM_138387.3:c.736C= , LRG_182t1:c.736C= NP_612396.1:p.Arg246=
NR_028581.1:n.1166C=
NR_028582.1:n.1031C=
XM_011525473.1:c.391C= XP_011523775.1:p.Arg131=
XM_011525474.1:c.391C= XP_011523776.1:p.Arg131=
NM_001319945.1:c.*29C= NP_001306874.1:n.*29C=
XM_011525473.3:c.391C= XP_011523775.1:p.Arg131=
XM_011525474.3:c.391C= XP_011523776.1:p.Arg131=
XM_017025335.2:c.391C= XP_016880824.1:p.Arg131=
NM_001319945.2:c.*29C= NP_001306874.1:n.*29C=
NR_028581.2:n.985C=
NR_028582.2:n.850C=
NM_001384165.1:c.391C= NP_001371094.1:p.Arg131=
NM_001384166.1:c.391C= NP_001371095.1:p.Arg131=
NM_001384167.1:c.391C= NP_001371096.1:p.Arg131=
NM_001384168.1:c.391C= NP_001371097.1:p.Arg131=
NM_138387.4:c.736C= MANE Select NP_612396.1:p.Arg246=