Canonical Allele Identifier: CA2260697489
Gene: G6PC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911321C= , CM000679.2:g.42911321C= GRCh38
NC_000017.10:g.41063338C= , CM000679.1:g.41063338C= GRCh37
NC_000017.9:g.38316864C= NCBI36
NG_011808.1:g.15524C= , LRG_147:g.15524C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.969C= MANE Select ENSP00000253801.1:p.Tyr323=
ENST00000253801.6:c.969C= ENSP00000253801.1:p.Tyr323=
ENST00000585489.1:c.*361C= ENSP00000466202.1:n.*361C=
ENST00000592383.5:c.*361C= ENSP00000465958.1:n.*361C=
NM_000151.3:c.969C= NP_000142.2:p.Tyr323=
NM_001270397.1:c.*361C= NP_001257326.1:n.*361C=
NM_000151.4:c.969C= MANE Select NP_000142.2:p.Tyr323=
NM_001270397.2:c.*361C= NP_001257326.1:n.*361C=