Canonical Allele Identifier: CA350436195

Gene: CPS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210647986C>G , CM000664.2:g.210647986C>G	GRCh38
NC_000002.11:g.211512710C>G , CM000664.1:g.211512710C>G	GRCh37
NC_000002.10:g.211220955C>G	NCBI36
NG_008285.1:g.175302C>G , LRG_336:g.175302C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.3265C>G MANE Select	ENSP00000233072.5:p.Arg1089Gly
ENST00000430249.7:c.3283C>G	ENSP00000402608.2:p.Arg1095Gly
ENST00000451903.3:c.1912C>G	ENSP00000406136.2:p.Arg638Gly
ENST00000673510.1:c.3265C>G	ENSP00000500537.1:p.Arg1089Gly
ENST00000673630.1:c.3265C>G	ENSP00000501073.1:p.Arg1089Gly
ENST00000673698.1:c.1745C>G
ENST00000673711.1:c.3265C>G	ENSP00000501022.1:p.Arg1089Gly
ENST00000674074.1:n.2410C>G
ENST00000233072.9:c.3265C>G	ENSP00000233072.5:p.Arg1089Gly
ENST00000430249.6:c.3283C>G	ENSP00000402608.2:p.Arg1095Gly
ENST00000451903.2:c.1912C>G	ENSP00000406136.2:p.Arg638Gly
NM_001122633.2:c.3283C>G	NP_001116105.1:p.Arg1095Gly
NM_001122634.3:c.1912C>G	NP_001116106.1:p.Arg638Gly
NM_001875.4:c.3265C>G , LRG_336t1:c.3265C>G	NP_001866.2:p.Arg1089Gly
XM_011510640.1:c.3298C>G	XP_011508942.1:p.Arg1100Gly
XM_011510641.1:c.3265C>G	XP_011508943.1:p.Arg1089Gly
XM_011510642.1:c.3265C>G	XP_011508944.1:p.Arg1089Gly
XM_011510643.1:c.3265C>G	XP_011508945.1:p.Arg1089Gly
XM_011510644.1:c.3265C>G	XP_011508946.1:p.Arg1089Gly
NM_001122633.3:c.3265C>G	NP_001116105.2:p.Arg1089Gly
NM_001369256.1:c.3298C>G	NP_001356185.1:p.Arg1100Gly
NM_001369257.1:c.3265C>G	NP_001356186.1:p.Arg1089Gly
NM_001875.5:c.3265C>G MANE Select	NP_001866.2:p.Arg1089Gly
NR_161225.1:n.4174C>G
NR_163592.1:n.2421C>G