Canonical Allele Identifier: CA290783610
Gene: G6PC1 HGNC NCBI

Linked Data

dbSNP Id: rs34960677
MyVariant Identifiers: chr17:g.41052885_41052886insA (hg19) chr17:g.42900868_42900869insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42900871dup , CM000679.2:g.42900871dup GRCh38
NC_000017.10:g.41052888dup , CM000679.1:g.41052888dup GRCh37
NC_000017.9:g.38306414dup NCBI36
NG_011808.1:g.5074dup , LRG_147:g.5074dup

Transcript Alleles

HGVS Amino-acid change
ENST00000253801.7:c.-6dup MANE Select ENSP00000253801.1:n.-6dup
ENST00000253801.6:c.-6dup ENSP00000253801.1:n.-6dup
ENST00000585489.1:c.-6dup ENSP00000466202.1:n.-6dup
ENST00000588481.1:n.60dup
ENST00000592383.5:c.-6dup ENSP00000465958.1:n.-6dup
NM_000151.3:c.-6dup NP_000142.2:n.-6dup
NM_001270397.1:c.-6dup NP_001257326.1:n.-6dup
NM_000151.4:c.-6dup MANE Select NP_000142.2:n.-6dup
NM_001270397.2:c.-6dup NP_001257326.1:n.-6dup
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