Canonical Allele Identifier: CA2260696754
Gene: G6PC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42909577T= , CM000679.2:g.42909577T= GRCh38
NC_000017.10:g.41061594T= , CM000679.1:g.41061594T= GRCh37
NC_000017.9:g.38315120T= NCBI36
NG_011808.1:g.13780T= , LRG_147:g.13780T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.562+159T= MANE Select ENSP00000253801.1:n.562+159T=
ENST00000253801.6:c.562+159T= ENSP00000253801.1:n.562+159T=
ENST00000585489.1:c.447-1338T= ENSP00000466202.1:n.447-1338T=
ENST00000592383.5:c.485+159T= ENSP00000465958.1:n.485+159T=
NM_000151.3:c.562+159T= NP_000142.2:n.562+159T=
NM_001270397.1:c.485+159T= NP_001257326.1:n.485+159T=
NM_000151.4:c.562+159T= MANE Select NP_000142.2:n.562+159T=
NM_001270397.2:c.485+159T= NP_001257326.1:n.485+159T=