Canonical Allele Identifier: CA2260697562
Gene: G6PC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911460A= , CM000679.2:g.42911460A= GRCh38
NC_000017.10:g.41063477A= , CM000679.1:g.41063477A= GRCh37
NC_000017.9:g.38317003A= NCBI36
NG_011808.1:g.15663A= , LRG_147:g.15663A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.*34A= MANE Select ENSP00000253801.1:n.*34A=
ENST00000253801.6:c.*34A= ENSP00000253801.1:n.*34A=
ENST00000585489.1:c.*500A= ENSP00000466202.1:n.*500A=
NM_000151.3:c.*34A= NP_000142.2:n.*34A=
NM_001270397.1:c.*500A= NP_001257326.1:n.*500A=
NM_000151.4:c.*34A= MANE Select NP_000142.2:n.*34A=
NM_001270397.2:c.*500A= NP_001257326.1:n.*500A=