Canonical Allele Identifier: CA500229381

Gene: G6PC1

Linked Data

• MyVariant Identifiers: chr17:g.41053064G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42901047G>T , CM000679.2:g.42901047G>T	GRCh38
NC_000017.10:g.41053064G>T , CM000679.1:g.41053064G>T	GRCh37
NC_000017.9:g.38306590G>T	NCBI36
NG_011808.1:g.5250G>T , LRG_147:g.5250G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253801.7:c.171G>T MANE Select	ENSP00000253801.1:p.Val57=
ENST00000253801.6:c.171G>T	ENSP00000253801.1:p.Val57=
ENST00000585489.1:c.171G>T	ENSP00000466202.1:p.Val57=
ENST00000588481.1:n.236G>T
ENST00000592383.5:c.171G>T	ENSP00000465958.1:p.Val57=
NM_000151.3:c.171G>T	NP_000142.2:p.Val57=
NM_001270397.1:c.171G>T	NP_001257326.1:p.Val57=
NM_000151.4:c.171G>T MANE Select	NP_000142.2:p.Val57=
NM_001270397.2:c.171G>T	NP_001257326.1:p.Val57=