Canonical Allele Identifier: CA399650048
Gene: G6PC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42900925C>A , CM000679.2:g.42900925C>A GRCh38
NC_000017.10:g.41052942C>A , CM000679.1:g.41052942C>A GRCh37
NC_000017.9:g.38306468C>A NCBI36
NG_011808.1:g.5128C>A , LRG_147:g.5128C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.49C>A MANE Select ENSP00000253801.1:p.His17Asn
ENST00000253801.6:c.49C>A ENSP00000253801.1:p.His17Asn
ENST00000585489.1:c.49C>A ENSP00000466202.1:p.His17Asn
ENST00000588481.1:n.114C>A
ENST00000592383.5:c.49C>A ENSP00000465958.1:p.His17Asn
NM_000151.3:c.49C>A NP_000142.2:p.His17Asn
NM_001270397.1:c.49C>A NP_001257326.1:p.His17Asn
NM_000151.4:c.49C>A MANE Select NP_000142.2:p.His17Asn
NM_001270397.2:c.49C>A NP_001257326.1:p.His17Asn