Canonical Allele Identifier: CA431012805

Gene: CPS1

Linked Data

• ClinVar Variation Id: 2804048
• ClinVar RCV Id: RCV003604051
• dbSNP Id: rs1184105655
• MyVariant Identifiers: chr2:g.211473100C>T (hg19) ; chr2:g.210608376C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210608376C>T , CM000664.2:g.210608376C>T	GRCh38
NC_000002.11:g.211473100C>T , CM000664.1:g.211473100C>T	GRCh37
NC_000002.10:g.211181345C>T	NCBI36
NG_008285.1:g.135692C>T , LRG_336:g.135692C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.2208C>T MANE Select	ENSP00000233072.5:p.Phe736=
ENST00000430249.7:c.2226C>T	ENSP00000402608.2:p.Phe742=
ENST00000451903.3:c.855C>T	ENSP00000406136.2:p.Phe285=
ENST00000673510.1:c.2208C>T	ENSP00000500537.1:p.Phe736=
ENST00000673630.1:c.2208C>T	ENSP00000501073.1:p.Phe736=
ENST00000673698.1:c.688C>T
ENST00000673711.1:c.2208C>T	ENSP00000501022.1:p.Phe736=
ENST00000674074.1:n.1353C>T
ENST00000233072.9:c.2208C>T	ENSP00000233072.5:p.Phe736=
ENST00000430249.6:c.2226C>T	ENSP00000402608.2:p.Phe742=
ENST00000451903.2:c.855C>T	ENSP00000406136.2:p.Phe285=
NM_001122633.2:c.2226C>T	NP_001116105.1:p.Phe742=
NM_001122634.3:c.855C>T	NP_001116106.1:p.Phe285=
NM_001875.4:c.2208C>T , LRG_336t1:c.2208C>T	NP_001866.2:p.Phe736=
XM_011510640.1:c.2241C>T	XP_011508942.1:p.Phe747=
XM_011510641.1:c.2208C>T	XP_011508943.1:p.Phe736=
XM_011510642.1:c.2208C>T	XP_011508944.1:p.Phe736=
XM_011510643.1:c.2208C>T	XP_011508945.1:p.Phe736=
XM_011510644.1:c.2208C>T	XP_011508946.1:p.Phe736=
NM_001122633.3:c.2208C>T	NP_001116105.2:p.Phe736=
NM_001369256.1:c.2241C>T	NP_001356185.1:p.Phe747=
NM_001369257.1:c.2208C>T	NP_001356186.1:p.Phe736=
NM_001875.5:c.2208C>T MANE Select	NP_001866.2:p.Phe736=
NR_161225.1:n.3117C>T
NR_163592.1:n.1364C>T