Canonical Allele Identifier: CA2260697559
Gene: G6PC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911452A= , CM000679.2:g.42911452A= GRCh38
NC_000017.10:g.41063469A= , CM000679.1:g.41063469A= GRCh37
NC_000017.9:g.38316995A= NCBI36
NG_011808.1:g.15655A= , LRG_147:g.15655A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.*26A= MANE Select ENSP00000253801.1:n.*26A=
ENST00000253801.6:c.*26A= ENSP00000253801.1:n.*26A=
ENST00000585489.1:c.*492A= ENSP00000466202.1:n.*492A=
NM_000151.3:c.*26A= NP_000142.2:n.*26A=
NM_001270397.1:c.*492A= NP_001257326.1:n.*492A=
NM_000151.4:c.*26A= MANE Select NP_000142.2:n.*26A=
NM_001270397.2:c.*492A= NP_001257326.1:n.*492A=