Canonical Allele Identifier: CA399654962

Gene: G6PC1

Linked Data

• MyVariant Identifiers: chr17:g.41061396G>T (hg19) ; chr17:g.42909379G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42909379G>T , CM000679.2:g.42909379G>T	GRCh38
NC_000017.10:g.41061396G>T , CM000679.1:g.41061396G>T	GRCh37
NC_000017.9:g.38314922G>T	NCBI36
NG_011808.1:g.13582G>T , LRG_147:g.13582G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253801.7:c.523G>T MANE Select	ENSP00000253801.1:p.Ala175Ser
ENST00000253801.6:c.523G>T	ENSP00000253801.1:p.Ala175Ser
ENST00000585489.1:c.447-1536G>T	ENSP00000466202.1:n.447-1536G>T
ENST00000592383.5:c.446G>T	ENSP00000465958.1:p.Cys149Phe
NM_000151.3:c.523G>T	NP_000142.2:p.Ala175Ser
NM_001270397.1:c.446G>T	NP_001257326.1:p.Cys149Phe
NM_000151.4:c.523G>T MANE Select	NP_000142.2:p.Ala175Ser
NM_001270397.2:c.446G>T	NP_001257326.1:p.Cys149Phe