Canonical Allele Identifier: CA431012837

Gene: CPS1

Linked Data

• ClinVar Variation Id: 2124507
• ClinVar RCV Id: RCV003057196
• gnomAD v4: 2-210608412-A-G
• MyVariant Identifiers: chr2:g.211473136A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210608412A>G , CM000664.2:g.210608412A>G	GRCh38
NC_000002.11:g.211473136A>G , CM000664.1:g.211473136A>G	GRCh37
NC_000002.10:g.211181381A>G	NCBI36
NG_008285.1:g.135728A>G , LRG_336:g.135728A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.2244A>G MANE Select	ENSP00000233072.5:p.Pro748=
ENST00000430249.7:c.2262A>G	ENSP00000402608.2:p.Pro754=
ENST00000451903.3:c.891A>G	ENSP00000406136.2:p.Pro297=
ENST00000673510.1:c.2244A>G	ENSP00000500537.1:p.Pro748=
ENST00000673630.1:c.2244A>G	ENSP00000501073.1:p.Pro748=
ENST00000673698.1:c.724A>G
ENST00000673711.1:c.2244A>G	ENSP00000501022.1:p.Pro748=
ENST00000674074.1:n.1389A>G
ENST00000233072.9:c.2244A>G	ENSP00000233072.5:p.Pro748=
ENST00000430249.6:c.2262A>G	ENSP00000402608.2:p.Pro754=
ENST00000451903.2:c.891A>G	ENSP00000406136.2:p.Pro297=
NM_001122633.2:c.2262A>G	NP_001116105.1:p.Pro754=
NM_001122634.3:c.891A>G	NP_001116106.1:p.Pro297=
NM_001875.4:c.2244A>G , LRG_336t1:c.2244A>G	NP_001866.2:p.Pro748=
XM_011510640.1:c.2277A>G	XP_011508942.1:p.Pro759=
XM_011510641.1:c.2244A>G	XP_011508943.1:p.Pro748=
XM_011510642.1:c.2244A>G	XP_011508944.1:p.Pro748=
XM_011510643.1:c.2244A>G	XP_011508945.1:p.Pro748=
XM_011510644.1:c.2244A>G	XP_011508946.1:p.Pro748=
NM_001122633.3:c.2244A>G	NP_001116105.2:p.Pro748=
NM_001369256.1:c.2277A>G	NP_001356185.1:p.Pro759=
NM_001369257.1:c.2244A>G	NP_001356186.1:p.Pro748=
NM_001875.5:c.2244A>G MANE Select	NP_001866.2:p.Pro748=
NR_161225.1:n.3153A>G
NR_163592.1:n.1400A>G