Canonical Allele Identifier: CA2260696642
Gene: G6PC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42909335G= , CM000679.2:g.42909335G= GRCh38
NC_000017.10:g.41061352G= , CM000679.1:g.41061352G= GRCh37
NC_000017.9:g.38314878G= NCBI36
NG_011808.1:g.13538G= , LRG_147:g.13538G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.479G= MANE Select ENSP00000253801.1:p.Trp160=
ENST00000253801.6:c.479G= ENSP00000253801.1:p.Trp160=
ENST00000585489.1:c.447-1580G= ENSP00000466202.1:n.447-1580G=
ENST00000592383.5:c.402G= ENSP00000465958.1:p.Leu134=
NM_000151.3:c.479G= NP_000142.2:p.Trp160=
NM_001270397.1:c.402G= NP_001257326.1:p.Leu134=
NM_000151.4:c.479G= MANE Select NP_000142.2:p.Trp160=
NM_001270397.2:c.402G= NP_001257326.1:p.Leu134=