Canonical Allele Identifier: CA399729278

Gene: G6PC3

Linked Data

• gnomAD v4: 17-44075766-C-T
• MyVariant Identifiers: chr17:g.42153134C>T (hg19) ; chr17:g.44075766C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44075766C>T , CM000679.2:g.44075766C>T	GRCh38
NC_000017.10:g.42153134C>T , CM000679.1:g.42153134C>T	GRCh37
NC_000017.9:g.39508660C>T	NCBI36
NG_015818.1:g.10037C>T , LRG_182:g.10037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585361.6:c.*601C>T	ENSP00000466983.1:n.*601C>T
ENST00000588558.6:c.*739C>T	ENSP00000467624.1:n.*739C>T
ENST00000590253.3:c.*57C>T	ENSP00000465111.2:n.*57C>T
ENST00000593115.2:c.*785C>T	ENSP00000466821.1:n.*785C>T
ENST00000696383.1:c.419C>T	ENSP00000512593.1:p.Ser140Leu
ENST00000696384.1:c.*324C>T	ENSP00000512594.1:n.*324C>T
ENST00000696385.1:c.*482C>T	ENSP00000512595.1:n.*482C>T
ENST00000696386.1:c.*57C>T	ENSP00000512596.1:n.*57C>T
ENST00000696387.1:c.*391C>T	ENSP00000512597.1:n.*391C>T
ENST00000696388.1:c.*610C>T	ENSP00000512598.1:n.*610C>T
ENST00000696389.1:c.*795C>T	ENSP00000512599.1:n.*795C>T
ENST00000696390.1:c.554C>T	ENSP00000512600.1:p.Ser185Leu
ENST00000696391.1:c.*620C>T	ENSP00000512601.1:n.*620C>T
ENST00000696392.1:c.764C>T	ENSP00000512602.1:p.Ser255Leu
ENST00000696393.1:c.764C>T	ENSP00000512603.1:p.Ser255Leu
ENST00000696405.1:c.677+315C>T	ENSP00000512607.1:n.677+315C>T
ENST00000269097.9:c.764C>T MANE Select	ENSP00000269097.3:p.Ser255Leu
ENST00000269097.8:c.764C>T	ENSP00000269097.3:p.Ser255Leu
ENST00000585361.5:c.*601C>T	ENSP00000466983.1:n.*601C>T
ENST00000588558.5:c.*739C>T	ENSP00000467624.1:n.*739C>T
ENST00000590253.2:c.266C>T
ENST00000590639.1:n.785C>T
ENST00000591696.1:c.656C>T	ENSP00000468677.1:p.Ser219Leu
NM_138387.3:c.764C>T , LRG_182t1:c.764C>T	NP_612396.1:p.Ser255Leu
NR_028581.1:n.1194C>T
NR_028582.1:n.1059C>T
XM_011525473.1:c.419C>T	XP_011523775.1:p.Ser140Leu
XM_011525474.1:c.419C>T	XP_011523776.1:p.Ser140Leu
NM_001319945.1:c.*57C>T	NP_001306874.1:n.*57C>T
XM_011525473.3:c.419C>T	XP_011523775.1:p.Ser140Leu
XM_011525474.3:c.419C>T	XP_011523776.1:p.Ser140Leu
XM_017025335.2:c.419C>T	XP_016880824.1:p.Ser140Leu
NM_001319945.2:c.*57C>T	NP_001306874.1:n.*57C>T
NR_028581.2:n.1013C>T
NR_028582.2:n.878C>T
NM_001384165.1:c.419C>T	NP_001371094.1:p.Ser140Leu
NM_001384166.1:c.419C>T	NP_001371095.1:p.Ser140Leu
NM_001384167.1:c.419C>T	NP_001371096.1:p.Ser140Leu
NM_001384168.1:c.419C>T	NP_001371097.1:p.Ser140Leu
NM_138387.4:c.764C>T MANE Select	NP_612396.1:p.Ser255Leu