Canonical Allele Identifier: CA399729104
Gene: G6PC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44075687A>T , CM000679.2:g.44075687A>T GRCh38
NC_000017.10:g.42153055A>T , CM000679.1:g.42153055A>T GRCh37
NC_000017.9:g.39508581A>T NCBI36
NG_015818.1:g.9958A>T , LRG_182:g.9958A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000585361.6:c.*522A>T ENSP00000466983.1:n.*522A>T
ENST00000588558.6:c.*660A>T ENSP00000467624.1:n.*660A>T
ENST00000590253.3:c.566A>T ENSP00000465111.2:p.Gln189Leu
ENST00000593115.2:c.*706A>T ENSP00000466821.1:n.*706A>T
ENST00000696383.1:c.340A>T ENSP00000512593.1:p.Ser114Cys
ENST00000696384.1:c.*245A>T ENSP00000512594.1:n.*245A>T
ENST00000696385.1:c.*403A>T ENSP00000512595.1:n.*403A>T
ENST00000696386.1:c.368A>T ENSP00000512596.1:p.Gln123Leu
ENST00000696387.1:c.*312A>T ENSP00000512597.1:n.*312A>T
ENST00000696388.1:c.*531A>T ENSP00000512598.1:n.*531A>T
ENST00000696389.1:c.*716A>T ENSP00000512599.1:n.*716A>T
ENST00000696390.1:c.475A>T ENSP00000512600.1:p.Ser159Cys
ENST00000696391.1:c.*541A>T ENSP00000512601.1:n.*541A>T
ENST00000696392.1:c.685A>T ENSP00000512602.1:p.Ser229Cys
ENST00000696393.1:c.685A>T ENSP00000512603.1:p.Ser229Cys
ENST00000696405.1:c.677+236A>T ENSP00000512607.1:n.677+236A>T
ENST00000269097.9:c.685A>T MANE Select ENSP00000269097.3:p.Ser229Cys
ENST00000269097.8:c.685A>T ENSP00000269097.3:p.Ser229Cys
ENST00000585361.5:c.*522A>T ENSP00000466983.1:n.*522A>T
ENST00000588558.5:c.*660A>T ENSP00000467624.1:n.*660A>T
ENST00000590253.2:c.187A>T
ENST00000590639.1:n.706A>T
ENST00000591696.1:c.577A>T ENSP00000468677.1:p.Ser193Cys
NM_138387.3:c.685A>T , LRG_182t1:c.685A>T NP_612396.1:p.Ser229Cys
NR_028581.1:n.1115A>T
NR_028582.1:n.980A>T
XM_006722179.2:c.566A>T XP_006722242.1:p.Gln189Leu
XM_011525473.1:c.340A>T XP_011523775.1:p.Ser114Cys
XM_011525474.1:c.340A>T XP_011523776.1:p.Ser114Cys
NM_001319945.1:c.566A>T NP_001306874.1:p.Gln189Leu
XM_011525473.3:c.340A>T XP_011523775.1:p.Ser114Cys
XM_011525474.3:c.340A>T XP_011523776.1:p.Ser114Cys
XM_017025335.2:c.340A>T XP_016880824.1:p.Ser114Cys
NM_001319945.2:c.566A>T NP_001306874.1:p.Gln189Leu
NR_028581.2:n.934A>T
NR_028582.2:n.799A>T
NM_001384165.1:c.340A>T NP_001371094.1:p.Ser114Cys
NM_001384166.1:c.340A>T NP_001371095.1:p.Ser114Cys
NM_001384167.1:c.340A>T NP_001371096.1:p.Ser114Cys
NM_001384168.1:c.340A>T NP_001371097.1:p.Ser114Cys
NM_138387.4:c.685A>T MANE Select NP_612396.1:p.Ser229Cys