Canonical Allele Identifier: CA324941
Gene: G6PC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 214462
dbSNP Id: rs863224022

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911317T>A , CM000679.2:g.42911317T>A GRCh38
NC_000017.10:g.41063334T>A , CM000679.1:g.41063334T>A GRCh37
NC_000017.9:g.38316860T>A NCBI36
NG_011808.1:g.15520T>A , LRG_147:g.15520T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.965T>A MANE Select ENSP00000253801.1:p.Phe322Tyr
ENST00000253801.6:c.965T>A ENSP00000253801.1:p.Phe322Tyr
ENST00000585489.1:c.*357T>A ENSP00000466202.1:n.*357T>A
ENST00000592383.5:c.*357T>A ENSP00000465958.1:n.*357T>A
NM_000151.3:c.965T>A NP_000142.2:p.Phe322Tyr
NM_001270397.1:c.*357T>A NP_001257326.1:n.*357T>A
NM_000151.4:c.965T>A MANE Select NP_000142.2:p.Phe322Tyr
NM_001270397.2:c.*357T>A NP_001257326.1:n.*357T>A