Canonical Allele Identifier: CA1041902063
Gene: CPS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.210608571_210608573del , CM000664.2:g.210608571_210608573del GRCh38
NC_000002.11:g.211473295_211473297del , CM000664.1:g.211473295_211473297del GRCh37
NC_000002.10:g.211181540_211181542del NCBI36
NG_008285.1:g.135887_135889del , LRG_336:g.135887_135889del

Transcript Alleles

HGVS Amino-acid Change
ENST00000233072.10:c.2391+12_2391+14del MANE Select ENSP00000233072.5:n.2391+12_2391+14del
ENST00000430249.7:c.2409+12_2409+14del ENSP00000402608.2:n.2409+12_2409+14del
ENST00000451903.3:c.1038+12_1038+14del ENSP00000406136.2:n.1038+12_1038+14del
ENST00000673510.1:c.2391+12_2391+14del ENSP00000500537.1:n.2391+12_2391+14del
ENST00000673630.1:c.2391+12_2391+14del ENSP00000501073.1:n.2391+12_2391+14del
ENST00000673698.1:c.871+12_871+14del
ENST00000673711.1:c.2391+12_2391+14del ENSP00000501022.1:n.2391+12_2391+14del
ENST00000674074.1:n.1536+12_1536+14del
ENST00000233072.9:c.2391+12_2391+14del ENSP00000233072.5:n.2391+12_2391+14del
ENST00000430249.6:c.2409+12_2409+14del ENSP00000402608.2:n.2409+12_2409+14del
ENST00000451903.2:c.1038+12_1038+14del ENSP00000406136.2:n.1038+12_1038+14del
NM_001122633.2:c.2409+12_2409+14del NP_001116105.1:n.2409+12_2409+14del
NM_001122634.3:c.1038+12_1038+14del NP_001116106.1:n.1038+12_1038+14del
NM_001875.4:c.2391+12_2391+14del , LRG_336t1:c.2391+12_2391+14del NP_001866.2:n.2391+12_2391+14del
XM_011510640.1:c.2424+12_2424+14del XP_011508942.1:n.2424+12_2424+14del
XM_011510641.1:c.2391+12_2391+14del XP_011508943.1:n.2391+12_2391+14del
XM_011510642.1:c.2391+12_2391+14del XP_011508944.1:n.2391+12_2391+14del
XM_011510643.1:c.2391+12_2391+14del XP_011508945.1:n.2391+12_2391+14del
XM_011510644.1:c.2391+12_2391+14del XP_011508946.1:n.2391+12_2391+14del
NM_001122633.3:c.2391+12_2391+14del NP_001116105.2:n.2391+12_2391+14del
NM_001369256.1:c.2424+12_2424+14del NP_001356185.1:n.2424+12_2424+14del
NM_001369257.1:c.2391+12_2391+14del NP_001356186.1:n.2391+12_2391+14del
NM_001875.5:c.2391+12_2391+14del MANE Select NP_001866.2:n.2391+12_2391+14del
NR_161225.1:n.3300+12_3300+14del
NR_163592.1:n.1547+12_1547+14del