Canonical Allele Identifier: CA2086599

Gene: CPS1

Linked Data

• ClinVar Variation Id: 2181789
• ClinVar RCV Id: RCV002595836
• dbSNP Id: rs773998721
• ExAC: 2:211473158 G / A
• gnomAD v2: 2-211473158-G-A
• gnomAD v3: 2-210608434-G-A
• gnomAD v4: 2-210608434-G-A
• MyVariant Identifiers: chr2:g.211473158G>A (hg19) ; chr2:g.210608434G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210608434G>A , CM000664.2:g.210608434G>A	GRCh38
NC_000002.11:g.211473158G>A , CM000664.1:g.211473158G>A	GRCh37
NC_000002.10:g.211181403G>A	NCBI36
NG_008285.1:g.135750G>A , LRG_336:g.135750G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.2266G>A MANE Select	ENSP00000233072.5:p.Gly756Arg
ENST00000430249.7:c.2284G>A	ENSP00000402608.2:p.Gly762Arg
ENST00000451903.3:c.913G>A	ENSP00000406136.2:p.Gly305Arg
ENST00000673510.1:c.2266G>A	ENSP00000500537.1:p.Gly756Arg
ENST00000673630.1:c.2266G>A	ENSP00000501073.1:p.Gly756Arg
ENST00000673698.1:c.746G>A
ENST00000673711.1:c.2266G>A	ENSP00000501022.1:p.Gly756Arg
ENST00000674074.1:n.1411G>A
ENST00000233072.9:c.2266G>A	ENSP00000233072.5:p.Gly756Arg
ENST00000430249.6:c.2284G>A	ENSP00000402608.2:p.Gly762Arg
ENST00000451903.2:c.913G>A	ENSP00000406136.2:p.Gly305Arg
NM_001122633.2:c.2284G>A	NP_001116105.1:p.Gly762Arg
NM_001122634.3:c.913G>A	NP_001116106.1:p.Gly305Arg
NM_001875.4:c.2266G>A , LRG_336t1:c.2266G>A	NP_001866.2:p.Gly756Arg
XM_011510640.1:c.2299G>A	XP_011508942.1:p.Gly767Arg
XM_011510641.1:c.2266G>A	XP_011508943.1:p.Gly756Arg
XM_011510642.1:c.2266G>A	XP_011508944.1:p.Gly756Arg
XM_011510643.1:c.2266G>A	XP_011508945.1:p.Gly756Arg
XM_011510644.1:c.2266G>A	XP_011508946.1:p.Gly756Arg
NM_001122633.3:c.2266G>A	NP_001116105.2:p.Gly756Arg
NM_001369256.1:c.2299G>A	NP_001356185.1:p.Gly767Arg
NM_001369257.1:c.2266G>A	NP_001356186.1:p.Gly756Arg
NM_001875.5:c.2266G>A MANE Select	NP_001866.2:p.Gly756Arg
NR_161225.1:n.3175G>A
NR_163592.1:n.1422G>A