Canonical Allele Identifier: CA399654969

Gene: G6PC1

Linked Data

• MyVariant Identifiers: chr17:g.41061399C>A (hg19) ; chr17:g.42909382C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42909382C>A , CM000679.2:g.42909382C>A	GRCh38
NC_000017.10:g.41061399C>A , CM000679.1:g.41061399C>A	GRCh37
NC_000017.9:g.38314925C>A	NCBI36
NG_011808.1:g.13585C>A , LRG_147:g.13585C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253801.7:c.526C>A MANE Select	ENSP00000253801.1:p.His176Asn
ENST00000253801.6:c.526C>A	ENSP00000253801.1:p.His176Asn
ENST00000585489.1:c.447-1533C>A	ENSP00000466202.1:n.447-1533C>A
ENST00000592383.5:c.449C>A	ENSP00000465958.1:p.Ser150Ter
NM_000151.3:c.526C>A	NP_000142.2:p.His176Asn
NM_001270397.1:c.449C>A	NP_001257326.1:p.Ser150Ter
NM_000151.4:c.526C>A MANE Select	NP_000142.2:p.His176Asn
NM_001270397.2:c.449C>A	NP_001257326.1:p.Ser150Ter