Canonical Allele Identifier: CA2638039941
Gene: G6PC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42903863T>A , CM000679.2:g.42903863T>A GRCh38
NC_000017.10:g.41055880T>A , CM000679.1:g.41055880T>A GRCh37
NC_000017.9:g.38309406T>A NCBI36
NG_011808.1:g.8066T>A , LRG_147:g.8066T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000253801.7:c.231-68T>A MANE Select ENSP00000253801.1:n.231-68T>A
ENST00000253801.6:c.231-68T>A ENSP00000253801.1:n.231-68T>A
ENST00000585489.1:c.231-68T>A ENSP00000466202.1:n.231-68T>A
ENST00000588481.1:n.296-68T>A
ENST00000592383.5:c.231-68T>A ENSP00000465958.1:n.231-68T>A
NM_000151.3:c.231-68T>A NP_000142.2:n.231-68T>A
NM_001270397.1:c.231-68T>A NP_001257326.1:n.231-68T>A
NM_000151.4:c.231-68T>A MANE Select NP_000142.2:n.231-68T>A
NM_001270397.2:c.231-68T>A NP_001257326.1:n.231-68T>A