Canonical Allele Identifier: CA2260696729
Gene: G6PC1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42909497A= , CM000679.2:g.42909497A= GRCh38
NC_000017.10:g.41061514A= , CM000679.1:g.41061514A= GRCh37
NC_000017.9:g.38315040A= NCBI36
NG_011808.1:g.13700A= , LRG_147:g.13700A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.562+79A= MANE Select ENSP00000253801.1:n.562+79A=
ENST00000253801.6:c.562+79A= ENSP00000253801.1:n.562+79A=
ENST00000585489.1:c.447-1418A= ENSP00000466202.1:n.447-1418A=
ENST00000592383.5:c.485+79A= ENSP00000465958.1:n.485+79A=
NM_000151.3:c.562+79A= NP_000142.2:n.562+79A=
NM_001270397.1:c.485+79A= NP_001257326.1:n.485+79A=
NM_000151.4:c.562+79A= MANE Select NP_000142.2:n.562+79A=
NM_001270397.2:c.485+79A= NP_001257326.1:n.485+79A=
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