Canonical Allele Identifier: CA399656200

Gene: G6PC1

Linked Data

• gnomAD v4: 17-42911121-C-T
• MyVariant Identifiers: chr17:g.41063138C>T (hg19) ; chr17:g.42911121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42911121C>T , CM000679.2:g.42911121C>T	GRCh38
NC_000017.10:g.41063138C>T , CM000679.1:g.41063138C>T	GRCh37
NC_000017.9:g.38316664C>T	NCBI36
NG_011808.1:g.15324C>T , LRG_147:g.15324C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000253801.7:c.769C>T MANE Select	ENSP00000253801.1:p.Pro257Ser
ENST00000253801.6:c.769C>T	ENSP00000253801.1:p.Pro257Ser
ENST00000585489.1:c.*161C>T	ENSP00000466202.1:n.*161C>T
ENST00000592383.5:c.*161C>T	ENSP00000465958.1:n.*161C>T
NM_000151.3:c.769C>T	NP_000142.2:p.Pro257Ser
NM_001270397.1:c.*161C>T	NP_001257326.1:n.*161C>T
NM_000151.4:c.769C>T MANE Select	NP_000142.2:p.Pro257Ser
NM_001270397.2:c.*161C>T	NP_001257326.1:n.*161C>T