Canonical Allele Identifier: CA2261216600
Gene: G6PC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44075649C= , CM000679.2:g.44075649C= GRCh38
NC_000017.10:g.42153017C= , CM000679.1:g.42153017C= GRCh37
NC_000017.9:g.39508543C= NCBI36
NG_015818.1:g.9920C= , LRG_182:g.9920C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000585361.6:c.*515-31C= ENSP00000466983.1:n.*515-31C=
ENST00000588558.6:c.*653-31C= ENSP00000467624.1:n.*653-31C=
ENST00000590253.3:c.559-31C= ENSP00000465111.2:n.559-31C=
ENST00000593115.2:c.*699-31C= ENSP00000466821.1:n.*699-31C=
ENST00000696383.1:c.333-31C= ENSP00000512593.1:n.333-31C=
ENST00000696384.1:c.*238-31C= ENSP00000512594.1:n.*238-31C=
ENST00000696385.1:c.*396-31C= ENSP00000512595.1:n.*396-31C=
ENST00000696386.1:c.361-31C= ENSP00000512596.1:n.361-31C=
ENST00000696387.1:c.*305-31C= ENSP00000512597.1:n.*305-31C=
ENST00000696388.1:c.*524-31C= ENSP00000512598.1:n.*524-31C=
ENST00000696389.1:c.*709-31C= ENSP00000512599.1:n.*709-31C=
ENST00000696390.1:c.468-31C= ENSP00000512600.1:n.468-31C=
ENST00000696391.1:c.*534-31C= ENSP00000512601.1:n.*534-31C=
ENST00000696392.1:c.678-31C= ENSP00000512602.1:n.678-31C=
ENST00000696393.1:c.678-31C= ENSP00000512603.1:n.678-31C=
ENST00000696405.1:c.677+198C= ENSP00000512607.1:n.677+198C=
ENST00000269097.9:c.678-31C= MANE Select ENSP00000269097.3:n.678-31C=
ENST00000269097.8:c.678-31C= ENSP00000269097.3:n.678-31C=
ENST00000585361.5:c.*515-31C= ENSP00000466983.1:n.*515-31C=
ENST00000588558.5:c.*653-31C= ENSP00000467624.1:n.*653-31C=
ENST00000590253.2:c.180-31C=
ENST00000590639.1:n.699-31C=
ENST00000591696.1:c.570-31C= ENSP00000468677.1:n.570-31C=
NM_138387.3:c.678-31C= , LRG_182t1:c.678-31C= NP_612396.1:n.678-31C=
NR_028581.1:n.1108-31C=
NR_028582.1:n.973-31C=
XM_006722179.2:c.559-31C= XP_006722242.1:n.559-31C=
XM_011525473.1:c.333-31C= XP_011523775.1:n.333-31C=
XM_011525474.1:c.333-31C= XP_011523776.1:n.333-31C=
NM_001319945.1:c.559-31C= NP_001306874.1:n.559-31C=
XM_011525473.3:c.333-31C= XP_011523775.1:n.333-31C=
XM_011525474.3:c.333-31C= XP_011523776.1:n.333-31C=
XM_017025335.2:c.333-31C= XP_016880824.1:n.333-31C=
NM_001319945.2:c.559-31C= NP_001306874.1:n.559-31C=
NR_028581.2:n.927-31C=
NR_028582.2:n.792-31C=
NM_001384165.1:c.333-31C= NP_001371094.1:n.333-31C=
NM_001384166.1:c.333-31C= NP_001371095.1:n.333-31C=
NM_001384167.1:c.333-31C= NP_001371096.1:n.333-31C=
NM_001384168.1:c.333-31C= NP_001371097.1:n.333-31C=
NM_138387.4:c.678-31C= MANE Select NP_612396.1:n.678-31C=