Canonical Allele Identifier: CA399654966

Gene: G6PC1

Linked Data

• MyVariant Identifiers: chr17:g.41061398T>A (hg19) ; chr17:g.42909381T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42909381T>A , CM000679.2:g.42909381T>A	GRCh38
NC_000017.10:g.41061398T>A , CM000679.1:g.41061398T>A	GRCh37
NC_000017.9:g.38314924T>A	NCBI36
NG_011808.1:g.13584T>A , LRG_147:g.13584T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253801.7:c.525T>A MANE Select	ENSP00000253801.1:p.Ala175=
ENST00000253801.6:c.525T>A	ENSP00000253801.1:p.Ala175=
ENST00000585489.1:c.447-1534T>A	ENSP00000466202.1:n.447-1534T>A
ENST00000592383.5:c.448T>A	ENSP00000465958.1:p.Ser150Thr
NM_000151.3:c.525T>A	NP_000142.2:p.Ala175=
NM_001270397.1:c.448T>A	NP_001257326.1:p.Ser150Thr
NM_000151.4:c.525T>A MANE Select	NP_000142.2:p.Ala175=
NM_001270397.2:c.448T>A	NP_001257326.1:p.Ser150Thr