Canonical Allele Identifier: CA1325073321
Gene: CPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210592891G= , CM000664.2:g.210592891G= GRCh38
NC_000002.11:g.211457615G= , CM000664.1:g.211457615G= GRCh37
NC_000002.10:g.211165860G= NCBI36
NG_008285.1:g.120207G= , LRG_336:g.120207G=

Transcript Alleles

HGVS Amino-acid change
ENST00000233072.10:c.1099G= MANE Select ENSP00000233072.5:p.Glu367=
ENST00000430249.7:c.1117G= ENSP00000402608.2:p.Glu373=
ENST00000673510.1:c.1099G= ENSP00000500537.1:p.Glu367=
ENST00000673630.1:c.1099G= ENSP00000501073.1:p.Glu367=
ENST00000673711.1:c.1099G= ENSP00000501022.1:p.Glu367=
ENST00000233072.9:c.1099G= ENSP00000233072.5:p.Glu367=
ENST00000430249.6:c.1117G= ENSP00000402608.2:p.Glu373=
ENST00000619804.1:c.1099G= ENSP00000480517.1:p.Glu367=
NM_001122633.2:c.1117G= NP_001116105.1:p.Glu373=
NM_001875.4:c.1099G= , LRG_336t1:c.1099G= NP_001866.2:p.Glu367=
XM_011510640.1:c.1132G= XP_011508942.1:p.Glu378=
XM_011510641.1:c.1099G= XP_011508943.1:p.Glu367=
XM_011510642.1:c.1099G= XP_011508944.1:p.Glu367=
XM_011510643.1:c.1099G= XP_011508945.1:p.Glu367=
XM_011510644.1:c.1099G= XP_011508946.1:p.Glu367=
NM_001122633.3:c.1099G= NP_001116105.2:p.Glu367=
NM_001369256.1:c.1132G= NP_001356185.1:p.Glu378=
NM_001369257.1:c.1099G= NP_001356186.1:p.Glu367=
NM_001875.5:c.1099G= MANE Select NP_001866.2:p.Glu367=
NR_161225.1:n.2011G=