Canonical Allele Identifier: CA2261216632
Gene: G6PC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44075711C= , CM000679.2:g.44075711C= GRCh38
NC_000017.10:g.42153079C= , CM000679.1:g.42153079C= GRCh37
NC_000017.9:g.39508605C= NCBI36
NG_015818.1:g.9982C= , LRG_182:g.9982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585361.6:c.*546C= ENSP00000466983.1:n.*546C=
ENST00000588558.6:c.*684C= ENSP00000467624.1:n.*684C=
ENST00000590253.3:c.*2C= ENSP00000465111.2:n.*2C=
ENST00000593115.2:c.*730C= ENSP00000466821.1:n.*730C=
ENST00000696383.1:c.364C= ENSP00000512593.1:p.Arg122=
ENST00000696384.1:c.*269C= ENSP00000512594.1:n.*269C=
ENST00000696385.1:c.*427C= ENSP00000512595.1:n.*427C=
ENST00000696386.1:c.*2C= ENSP00000512596.1:n.*2C=
ENST00000696387.1:c.*336C= ENSP00000512597.1:n.*336C=
ENST00000696388.1:c.*555C= ENSP00000512598.1:n.*555C=
ENST00000696389.1:c.*740C= ENSP00000512599.1:n.*740C=
ENST00000696390.1:c.499C= ENSP00000512600.1:p.Arg167=
ENST00000696391.1:c.*565C= ENSP00000512601.1:n.*565C=
ENST00000696392.1:c.709C= ENSP00000512602.1:p.Arg237=
ENST00000696393.1:c.709C= ENSP00000512603.1:p.Arg237=
ENST00000696405.1:c.677+260C= ENSP00000512607.1:n.677+260C=
ENST00000269097.9:c.709C= MANE Select ENSP00000269097.3:p.Arg237=
ENST00000269097.8:c.709C= ENSP00000269097.3:p.Arg237=
ENST00000585361.5:c.*546C= ENSP00000466983.1:n.*546C=
ENST00000588558.5:c.*684C= ENSP00000467624.1:n.*684C=
ENST00000590253.2:c.211C=
ENST00000590639.1:n.730C=
ENST00000591696.1:c.601C= ENSP00000468677.1:p.Arg201=
NM_138387.3:c.709C= , LRG_182t1:c.709C= NP_612396.1:p.Arg237=
NR_028581.1:n.1139C=
NR_028582.1:n.1004C=
XM_006722179.2:c.*2C= XP_006722242.1:n.*2C=
XM_011525473.1:c.364C= XP_011523775.1:p.Arg122=
XM_011525474.1:c.364C= XP_011523776.1:p.Arg122=
NM_001319945.1:c.*2C= NP_001306874.1:n.*2C=
XM_011525473.3:c.364C= XP_011523775.1:p.Arg122=
XM_011525474.3:c.364C= XP_011523776.1:p.Arg122=
XM_017025335.2:c.364C= XP_016880824.1:p.Arg122=
NM_001319945.2:c.*2C= NP_001306874.1:n.*2C=
NR_028581.2:n.958C=
NR_028582.2:n.823C=
NM_001384165.1:c.364C= NP_001371094.1:p.Arg122=
NM_001384166.1:c.364C= NP_001371095.1:p.Arg122=
NM_001384167.1:c.364C= NP_001371096.1:p.Arg122=
NM_001384168.1:c.364C= NP_001371097.1:p.Arg122=
NM_138387.4:c.709C= MANE Select NP_612396.1:p.Arg237=