Canonical Allele Identifier: CA500229427

Gene: G6PC1

Linked Data

• gnomAD v4: 17-42911333-C-T
• COSMIC: COSM3795646
• MyVariant Identifiers: chr17:g.41063350C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42911333C>T , CM000679.2:g.42911333C>T	GRCh38
NC_000017.10:g.41063350C>T , CM000679.1:g.41063350C>T	GRCh37
NC_000017.9:g.38316876C>T	NCBI36
NG_011808.1:g.15536C>T , LRG_147:g.15536C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253801.7:c.981C>T MANE Select	ENSP00000253801.1:p.Phe327=
ENST00000253801.6:c.981C>T	ENSP00000253801.1:p.Phe327=
ENST00000585489.1:c.*373C>T	ENSP00000466202.1:n.*373C>T
ENST00000592383.5:c.*373C>T	ENSP00000465958.1:n.*373C>T
NM_000151.3:c.981C>T	NP_000142.2:p.Phe327=
NM_001270397.1:c.*373C>T	NP_001257326.1:n.*373C>T
NM_000151.4:c.981C>T MANE Select	NP_000142.2:p.Phe327=
NM_001270397.2:c.*373C>T	NP_001257326.1:n.*373C>T