Canonical Allele Identifier: CA1325072863
Gene: CPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210591913_210591915delinsACC , CM000664.2:g.210591913_210591915delinsACC GRCh38
NC_000002.11:g.211456637_211456639delinsACC , CM000664.1:g.211456637_211456639delinsACC GRCh37
NC_000002.10:g.211164882_211164884delinsACC NCBI36
NG_008285.1:g.119229_119231delinsACC , LRG_336:g.119229_119231delinsACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000233072.10:c.1030_1032delinsACC MANE Select ENSP00000233072.5:p.Thr344=
ENST00000430249.7:c.1048_1050delinsACC ENSP00000402608.2:p.Thr350=
ENST00000673510.1:c.1030_1032delinsACC ENSP00000500537.1:p.Thr344=
ENST00000673630.1:c.1030_1032delinsACC ENSP00000501073.1:p.Thr344=
ENST00000673711.1:c.1030_1032delinsACC ENSP00000501022.1:p.Thr344=
ENST00000233072.9:c.1030_1032delinsACC ENSP00000233072.5:p.Thr344=
ENST00000430249.6:c.1048_1050delinsACC ENSP00000402608.2:p.Thr350=
ENST00000619804.1:c.1030_1032delinsACC ENSP00000480517.1:p.Thr344=
NM_001122633.2:c.1048_1050delinsACC NP_001116105.1:p.Thr350=
NM_001875.4:c.1030_1032delinsACC , LRG_336t1:c.1030_1032delinsACC NP_001866.2:p.Thr344=
XM_011510640.1:c.1063_1065delinsACC XP_011508942.1:p.Thr355=
XM_011510641.1:c.1030_1032delinsACC XP_011508943.1:p.Thr344=
XM_011510642.1:c.1030_1032delinsACC XP_011508944.1:p.Thr344=
XM_011510643.1:c.1030_1032delinsACC XP_011508945.1:p.Thr344=
XM_011510644.1:c.1030_1032delinsACC XP_011508946.1:p.Thr344=
NM_001122633.3:c.1030_1032delinsACC NP_001116105.2:p.Thr344=
NM_001369256.1:c.1063_1065delinsACC NP_001356185.1:p.Thr355=
NM_001369257.1:c.1030_1032delinsACC NP_001356186.1:p.Thr344=
NM_001875.5:c.1030_1032delinsACC MANE Select NP_001866.2:p.Thr344=
NR_161225.1:n.1942_1944delinsACC