Canonical Allele Identifier: CA2261216652
Gene: G6PC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44075756_44075780delinsAGCCGTGACTCAGGGGCTGCCCTGG , CM000679.2:g.44075756_44075780delinsAGCCGTGACTCAGGGGCTGCCCTGG GRCh38
NC_000017.10:g.42153124_42153148delinsAGCCGTGACTCAGGGGCTGCCCTGG , CM000679.1:g.42153124_42153148delinsAGCCGTGACTCAGGGGCTGCCCTGG GRCh37
NC_000017.9:g.39508650_39508674delinsAGCCGTGACTCAGGGGCTGCCCTGG NCBI36
NG_015818.1:g.10027_10051delinsAGCCGTGACTCAGGGGCTGCCCTGG , LRG_182:g.10027_10051delinsAGCCGTGACTCAGGGGCTGCCCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000585361.6:c.*591_*615delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000466983.1:n.*591_*615delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000588558.6:c.*729_*753delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000467624.1:n.*729_*753delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000590253.3:c.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000465111.2:n.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000593115.2:c.*775_*799delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000466821.1:n.*775_*799delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696383.1:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512593.1:p.Ser137=
ENST00000696384.1:c.*314_*338delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512594.1:n.*314_*338delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696385.1:c.*472_*496delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512595.1:n.*472_*496delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696386.1:c.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512596.1:n.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696387.1:c.*381_*405delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512597.1:n.*381_*405delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696388.1:c.*600_*624delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512598.1:n.*600_*624delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696389.1:c.*785_*809delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512599.1:n.*785_*809delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696390.1:c.544_568delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512600.1:p.Ser182=
ENST00000696391.1:c.*610_*634delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512601.1:n.*610_*634delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000696392.1:c.754_778delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512602.1:p.Ser252=
ENST00000696393.1:c.754_778delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512603.1:p.Ser252=
ENST00000696405.1:c.677+305_677+329delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000512607.1:n.677+305_677+329delinsAGCCGTGACTCAGGGGCTGC...
ENST00000269097.9:c.754_778delinsAGCCGTGACTCAGGGGCTGCCCTGG MANE Select ENSP00000269097.3:p.Ser252=
ENST00000269097.8:c.754_778delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000269097.3:p.Ser252=
ENST00000585361.5:c.*591_*615delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000466983.1:n.*591_*615delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000588558.5:c.*729_*753delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000467624.1:n.*729_*753delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000590253.2:c.256_280delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000590639.1:n.775_799delinsAGCCGTGACTCAGGGGCTGCCCTGG
ENST00000591696.1:c.646_670delinsAGCCGTGACTCAGGGGCTGCCCTGG ENSP00000468677.1:p.Ser216=
NM_138387.3:c.754_778delinsAGCCGTGACTCAGGGGCTGCCCTGG , LRG_182t1:c.754_778delinsAGCCGTGACTCAGGGGCTGCCCTGG NP_612396.1:p.Ser252=
NR_028581.1:n.1184_1208delinsAGCCGTGACTCAGGGGCTGCCCTGG
NR_028582.1:n.1049_1073delinsAGCCGTGACTCAGGGGCTGCCCTGG
XM_011525473.1:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG XP_011523775.1:p.Ser137=
XM_011525474.1:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG XP_011523776.1:p.Ser137=
NM_001319945.1:c.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG NP_001306874.1:n.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG
XM_011525473.3:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG XP_011523775.1:p.Ser137=
XM_011525474.3:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG XP_011523776.1:p.Ser137=
XM_017025335.2:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG XP_016880824.1:p.Ser137=
NM_001319945.2:c.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG NP_001306874.1:n.*47_*71delinsAGCCGTGACTCAGGGGCTGCCCTGG
NR_028581.2:n.1003_1027delinsAGCCGTGACTCAGGGGCTGCCCTGG
NR_028582.2:n.868_892delinsAGCCGTGACTCAGGGGCTGCCCTGG
NM_001384165.1:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG NP_001371094.1:p.Ser137=
NM_001384166.1:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG NP_001371095.1:p.Ser137=
NM_001384167.1:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG NP_001371096.1:p.Ser137=
NM_001384168.1:c.409_433delinsAGCCGTGACTCAGGGGCTGCCCTGG NP_001371097.1:p.Ser137=
NM_138387.4:c.754_778delinsAGCCGTGACTCAGGGGCTGCCCTGG MANE Select NP_612396.1:p.Ser252=