Canonical Allele Identifier: CA2261216369

Gene: G6PC3

Linked Data

• dbSNP Id: rs2050066760

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075241G>C , CM000679.2:g.44075241G>C	GRCh38
NC_000017.10:g.42152609G>C , CM000679.1:g.42152609G>C	GRCh37
NC_000017.9:g.39508135G>C	NCBI36
NG_015818.1:g.9512G>C , LRG_182:g.9512G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000585361.6:c.*373-69G>C	ENSP00000466983.1:n.*373-69G>C
ENST00000588558.6:c.*511-69G>C	ENSP00000467624.1:n.*511-69G>C
ENST00000590253.3:c.417-69G>C	ENSP00000465111.2:n.417-69G>C
ENST00000593115.2:c.*557-69G>C	ENSP00000466821.1:n.*557-69G>C
ENST00000696383.1:c.191-69G>C	ENSP00000512593.1:n.191-69G>C
ENST00000696384.1:c.*96-69G>C	ENSP00000512594.1:n.*96-69G>C
ENST00000696385.1:c.*254-69G>C	ENSP00000512595.1:n.*254-69G>C
ENST00000696386.1:c.219-69G>C	ENSP00000512596.1:n.219-69G>C
ENST00000696387.1:c.*163-69G>C	ENSP00000512597.1:n.*163-69G>C
ENST00000696388.1:c.*382-69G>C	ENSP00000512598.1:n.*382-69G>C
ENST00000696389.1:c.*567-69G>C	ENSP00000512599.1:n.*567-69G>C
ENST00000696390.1:c.326-69G>C	ENSP00000512600.1:n.326-69G>C
ENST00000696391.1:c.*392-69G>C	ENSP00000512601.1:n.*392-69G>C
ENST00000696392.1:c.536-69G>C	ENSP00000512602.1:n.536-69G>C
ENST00000696393.1:c.536-69G>C	ENSP00000512603.1:n.536-69G>C
ENST00000696405.1:c.536-69G>C	ENSP00000512607.1:n.536-69G>C
ENST00000269097.9:c.536-69G>C MANE Select	ENSP00000269097.3:n.536-69G>C
ENST00000269097.8:c.536-69G>C	ENSP00000269097.3:n.536-69G>C
ENST00000585361.5:c.*373-69G>C	ENSP00000466983.1:n.*373-69G>C
ENST00000588558.5:c.*511-69G>C	ENSP00000467624.1:n.*511-69G>C
ENST00000590253.2:c.38-69G>C
ENST00000590639.1:n.488G>C
ENST00000591696.1:c.428-69G>C	ENSP00000468677.1:n.428-69G>C
NM_138387.3:c.536-69G>C , LRG_182t1:c.536-69G>C	NP_612396.1:n.536-69G>C
NR_028581.1:n.966-69G>C
NR_028582.1:n.831-69G>C
XM_006722179.2:c.417-69G>C	XP_006722242.1:n.417-69G>C
XM_011525473.1:c.191-69G>C	XP_011523775.1:n.191-69G>C
XM_011525474.1:c.191-69G>C	XP_011523776.1:n.191-69G>C
NM_001319945.1:c.417-69G>C	NP_001306874.1:n.417-69G>C
XM_011525473.3:c.191-69G>C	XP_011523775.1:n.191-69G>C
XM_011525474.3:c.191-69G>C	XP_011523776.1:n.191-69G>C
XM_017025335.2:c.191-69G>C	XP_016880824.1:n.191-69G>C
NM_001319945.2:c.417-69G>C	NP_001306874.1:n.417-69G>C
NR_028581.2:n.785-69G>C
NR_028582.2:n.650-69G>C
NM_001384165.1:c.191-69G>C	NP_001371094.1:n.191-69G>C
NM_001384166.1:c.191-69G>C	NP_001371095.1:n.191-69G>C
NM_001384167.1:c.191-69G>C	NP_001371096.1:n.191-69G>C
NM_001384168.1:c.191-69G>C	NP_001371097.1:n.191-69G>C
NM_138387.4:c.536-69G>C MANE Select	NP_612396.1:n.536-69G>C