Canonical Allele Identifier: CA2638039696
Gene: G6PC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42901118A>G , CM000679.2:g.42901118A>G GRCh38
NC_000017.10:g.41053135A>G , CM000679.1:g.41053135A>G GRCh37
NC_000017.9:g.38306661A>G NCBI36
NG_011808.1:g.5321A>G , LRG_147:g.5321A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000253801.7:c.230+12A>G MANE Select ENSP00000253801.1:n.230+12A>G
ENST00000253801.6:c.230+12A>G ENSP00000253801.1:n.230+12A>G
ENST00000585489.1:c.230+12A>G ENSP00000466202.1:n.230+12A>G
ENST00000588481.1:n.295+12A>G
ENST00000592383.5:c.230+12A>G ENSP00000465958.1:n.230+12A>G
NM_000151.3:c.230+12A>G NP_000142.2:n.230+12A>G
NM_001270397.1:c.230+12A>G NP_001257326.1:n.230+12A>G
NM_000151.4:c.230+12A>G MANE Select NP_000142.2:n.230+12A>G
NM_001270397.2:c.230+12A>G NP_001257326.1:n.230+12A>G