Canonical Allele Identifier: CA2260692848
Gene: G6PC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42900922A= , CM000679.2:g.42900922A= GRCh38
NC_000017.10:g.41052939A= , CM000679.1:g.41052939A= GRCh37
NC_000017.9:g.38306465A= NCBI36
NG_011808.1:g.5125A= , LRG_147:g.5125A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.46A= MANE Select ENSP00000253801.1:p.Thr16=
ENST00000253801.6:c.46A= ENSP00000253801.1:p.Thr16=
ENST00000585489.1:c.46A= ENSP00000466202.1:p.Thr16=
ENST00000588481.1:n.111A=
ENST00000592383.5:c.46A= ENSP00000465958.1:p.Thr16=
NM_000151.3:c.46A= NP_000142.2:p.Thr16=
NM_001270397.1:c.46A= NP_001257326.1:p.Thr16=
NM_000151.4:c.46A= MANE Select NP_000142.2:p.Thr16=
NM_001270397.2:c.46A= NP_001257326.1:p.Thr16=