Canonical Allele Identifier: CA1325073319
Gene: CPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210592889A= , CM000664.2:g.210592889A= GRCh38
NC_000002.11:g.211457613A= , CM000664.1:g.211457613A= GRCh37
NC_000002.10:g.211165858A= NCBI36
NG_008285.1:g.120205A= , LRG_336:g.120205A=

Transcript Alleles

HGVS Amino-acid change
ENST00000233072.10:c.1097A= MANE Select ENSP00000233072.5:p.His366=
ENST00000430249.7:c.1115A= ENSP00000402608.2:p.His372=
ENST00000673510.1:c.1097A= ENSP00000500537.1:p.His366=
ENST00000673630.1:c.1097A= ENSP00000501073.1:p.His366=
ENST00000673711.1:c.1097A= ENSP00000501022.1:p.His366=
ENST00000233072.9:c.1097A= ENSP00000233072.5:p.His366=
ENST00000430249.6:c.1115A= ENSP00000402608.2:p.His372=
ENST00000619804.1:c.1097A= ENSP00000480517.1:p.His366=
NM_001122633.2:c.1115A= NP_001116105.1:p.His372=
NM_001875.4:c.1097A= , LRG_336t1:c.1097A= NP_001866.2:p.His366=
XM_011510640.1:c.1130A= XP_011508942.1:p.His377=
XM_011510641.1:c.1097A= XP_011508943.1:p.His366=
XM_011510642.1:c.1097A= XP_011508944.1:p.His366=
XM_011510643.1:c.1097A= XP_011508945.1:p.His366=
XM_011510644.1:c.1097A= XP_011508946.1:p.His366=
NM_001122633.3:c.1097A= NP_001116105.2:p.His366=
NM_001369256.1:c.1130A= NP_001356185.1:p.His377=
NM_001369257.1:c.1097A= NP_001356186.1:p.His366=
NM_001875.5:c.1097A= MANE Select NP_001866.2:p.His366=
NR_161225.1:n.2009A=