Canonical Allele Identifier: CA2261216619

Gene: G6PC3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075685_44075686delinsTC , CM000679.2:g.44075685_44075686delinsTC	GRCh38
NC_000017.10:g.42153053_42153054delinsTC , CM000679.1:g.42153053_42153054delinsTC	GRCh37
NC_000017.9:g.39508579_39508580delinsTC	NCBI36
NG_015818.1:g.9956_9957delinsTC , LRG_182:g.9956_9957delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000585361.6:c.*520_*521delinsTC	ENSP00000466983.1:n.*520_*521delinsTC
ENST00000588558.6:c.*658_*659delinsTC	ENSP00000467624.1:n.*658_*659delinsTC
ENST00000590253.3:c.564_565delinsTC	ENSP00000465111.2:p.His188=
ENST00000593115.2:c.*704_*705delinsTC	ENSP00000466821.1:n.*704_*705delinsTC
ENST00000696383.1:c.338_339delinsTC	ENSP00000512593.1:p.Ile113=
ENST00000696384.1:c.*243_*244delinsTC	ENSP00000512594.1:n.*243_*244delinsTC
ENST00000696385.1:c.*401_*402delinsTC	ENSP00000512595.1:n.*401_*402delinsTC
ENST00000696386.1:c.366_367delinsTC	ENSP00000512596.1:p.His122=
ENST00000696387.1:c.*310_*311delinsTC	ENSP00000512597.1:n.*310_*311delinsTC
ENST00000696388.1:c.*529_*530delinsTC	ENSP00000512598.1:n.*529_*530delinsTC
ENST00000696389.1:c.*714_*715delinsTC	ENSP00000512599.1:n.*714_*715delinsTC
ENST00000696390.1:c.473_474delinsTC	ENSP00000512600.1:p.Ile158=
ENST00000696391.1:c.*539_*540delinsTC	ENSP00000512601.1:n.*539_*540delinsTC
ENST00000696392.1:c.683_684delinsTC	ENSP00000512602.1:p.Ile228=
ENST00000696393.1:c.683_684delinsTC	ENSP00000512603.1:p.Ile228=
ENST00000696405.1:c.677+234_677+235delinsTC	ENSP00000512607.1:n.677+234_677+235delins...
ENST00000269097.9:c.683_684delinsTC MANE Select	ENSP00000269097.3:p.Ile228=
ENST00000269097.8:c.683_684delinsTC	ENSP00000269097.3:p.Ile228=
ENST00000585361.5:c.*520_*521delinsTC	ENSP00000466983.1:n.*520_*521delinsTC
ENST00000588558.5:c.*658_*659delinsTC	ENSP00000467624.1:n.*658_*659delinsTC
ENST00000590253.2:c.185_186delinsTC
ENST00000590639.1:n.704_705delinsTC
ENST00000591696.1:c.575_576delinsTC	ENSP00000468677.1:p.Ile192=
NM_138387.3:c.683_684delinsTC , LRG_182t1:c.683_684delinsTC	NP_612396.1:p.Ile228=
NR_028581.1:n.1113_1114delinsTC
NR_028582.1:n.978_979delinsTC
XM_006722179.2:c.564_565delinsTC	XP_006722242.1:p.His188=
XM_011525473.1:c.338_339delinsTC	XP_011523775.1:p.Ile113=
XM_011525474.1:c.338_339delinsTC	XP_011523776.1:p.Ile113=
NM_001319945.1:c.564_565delinsTC	NP_001306874.1:p.His188=
XM_011525473.3:c.338_339delinsTC	XP_011523775.1:p.Ile113=
XM_011525474.3:c.338_339delinsTC	XP_011523776.1:p.Ile113=
XM_017025335.2:c.338_339delinsTC	XP_016880824.1:p.Ile113=
NM_001319945.2:c.564_565delinsTC	NP_001306874.1:p.His188=
NR_028581.2:n.932_933delinsTC
NR_028582.2:n.797_798delinsTC
NM_001384165.1:c.338_339delinsTC	NP_001371094.1:p.Ile113=
NM_001384166.1:c.338_339delinsTC	NP_001371095.1:p.Ile113=
NM_001384167.1:c.338_339delinsTC	NP_001371096.1:p.Ile113=
NM_001384168.1:c.338_339delinsTC	NP_001371097.1:p.Ile113=
NM_138387.4:c.683_684delinsTC MANE Select	NP_612396.1:p.Ile228=