Canonical Allele Identifier: CA399657850
Gene: G6PC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41063418G>A (hg19) chr17:g.42911401G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911401G>A , CM000679.2:g.42911401G>A GRCh38
NC_000017.10:g.41063418G>A , CM000679.1:g.41063418G>A GRCh37
NC_000017.9:g.38316944G>A NCBI36
NG_011808.1:g.15604G>A , LRG_147:g.15604G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.1049G>A MANE Select ENSP00000253801.1:p.Gly350Asp
ENST00000253801.6:c.1049G>A ENSP00000253801.1:p.Gly350Asp
ENST00000585489.1:c.*441G>A ENSP00000466202.1:n.*441G>A
NM_000151.3:c.1049G>A NP_000142.2:p.Gly350Asp
NM_001270397.1:c.*441G>A NP_001257326.1:n.*441G>A
NM_000151.4:c.1049G>A MANE Select NP_000142.2:p.Gly350Asp
NM_001270397.2:c.*441G>A NP_001257326.1:n.*441G>A
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