Canonical Allele Identifier: CA1325080016
Gene: CPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210608388G= , CM000664.2:g.210608388G= GRCh38
NC_000002.11:g.211473112G= , CM000664.1:g.211473112G= GRCh37
NC_000002.10:g.211181357G= NCBI36
NG_008285.1:g.135704G= , LRG_336:g.135704G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000233072.10:c.2220G= MANE Select ENSP00000233072.5:p.Lys740=
ENST00000430249.7:c.2238G= ENSP00000402608.2:p.Lys746=
ENST00000451903.3:c.867G= ENSP00000406136.2:p.Lys289=
ENST00000673510.1:c.2220G= ENSP00000500537.1:p.Lys740=
ENST00000673630.1:c.2220G= ENSP00000501073.1:p.Lys740=
ENST00000673698.1:c.700G=
ENST00000673711.1:c.2220G= ENSP00000501022.1:p.Lys740=
ENST00000674074.1:n.1365G=
ENST00000233072.9:c.2220G= ENSP00000233072.5:p.Lys740=
ENST00000430249.6:c.2238G= ENSP00000402608.2:p.Lys746=
ENST00000451903.2:c.867G= ENSP00000406136.2:p.Lys289=
NM_001122633.2:c.2238G= NP_001116105.1:p.Lys746=
NM_001122634.3:c.867G= NP_001116106.1:p.Lys289=
NM_001875.4:c.2220G= , LRG_336t1:c.2220G= NP_001866.2:p.Lys740=
XM_011510640.1:c.2253G= XP_011508942.1:p.Lys751=
XM_011510641.1:c.2220G= XP_011508943.1:p.Lys740=
XM_011510642.1:c.2220G= XP_011508944.1:p.Lys740=
XM_011510643.1:c.2220G= XP_011508945.1:p.Lys740=
XM_011510644.1:c.2220G= XP_011508946.1:p.Lys740=
NM_001122633.3:c.2220G= NP_001116105.2:p.Lys740=
NM_001369256.1:c.2253G= NP_001356185.1:p.Lys751=
NM_001369257.1:c.2220G= NP_001356186.1:p.Lys740=
NM_001875.5:c.2220G= MANE Select NP_001866.2:p.Lys740=
NR_161225.1:n.3129G=
NR_163592.1:n.1376G=