Canonical Allele Identifier: CA2260697397
Gene: G6PC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911116C= , CM000679.2:g.42911116C= GRCh38
NC_000017.10:g.41063133C= , CM000679.1:g.41063133C= GRCh37
NC_000017.9:g.38316659C= NCBI36
NG_011808.1:g.15319C= , LRG_147:g.15319C=

Transcript Alleles

HGVS Amino-acid change
ENST00000253801.7:c.764C= MANE Select ENSP00000253801.1:p.Thr255=
ENST00000253801.6:c.764C= ENSP00000253801.1:p.Thr255=
ENST00000585489.1:c.*156C= ENSP00000466202.1:n.*156C=
ENST00000592383.5:c.*156C= ENSP00000465958.1:n.*156C=
NM_000151.3:c.764C= NP_000142.2:p.Thr255=
NM_001270397.1:c.*156C= NP_001257326.1:n.*156C=
NM_000151.4:c.764C= MANE Select NP_000142.2:p.Thr255=
NM_001270397.2:c.*156C= NP_001257326.1:n.*156C=