Canonical Allele Identifier: CA2580086937
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 1984158
ClinVar RCV Id: RCV002756749

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100157321_100157322del , CM000675.2:g.100157321_100157322del GRCh38
NC_000013.10:g.100809575_100809576del , CM000675.1:g.100809575_100809576del GRCh37
NC_000013.9:g.99607576_99607577del NCBI36
NG_008768.1:g.73239_73240del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376285.6:c.449_450del MANE Select ENSP00000365462.1:p.Lys150ArgfsTer17
ENST00000636366.1:c.328_329del
ENST00000636420.1:c.328_329del
ENST00000636475.1:c.328_329del
ENST00000637358.1:c.328_329del
ENST00000637657.1:c.328_329del
ENST00000647303.1:c.*297_*298del ENSP00000495663.1:n.*297_*298del
ENST00000376279.7:c.449_450del ENSP00000365456.3:p.Lys150ArgfsTer17
ENST00000376285.5:c.449_450del ENSP00000365462.1:p.Lys150ArgfsTer17
ENST00000376286.8:c.371_372del ENSP00000365463.4:p.Lys124ArgfsTer17
ENST00000485946.1:n.817_818del
NM_000282.3:c.449_450del NP_000273.2:p.Lys150ArgfsTer17
NM_001127692.2:c.371_372del NP_001121164.1:p.Lys124ArgfsTer17
NM_001178004.1:c.449_450del NP_001171475.1:p.Lys150ArgfsTer17
XM_005254059.2:c.449_450del XP_005254116.1:p.Lys150ArgfsTer17
XM_011521093.1:c.449_450del XP_011519395.1:p.Lys150ArgfsTer17
XR_931615.1:n.550_551del
XR_931616.1:n.550_551del
NM_001352605.1:c.449_450del NP_001339534.1:p.Lys150ArgfsTer17
NM_001352606.1:c.449_450del NP_001339535.1:p.Lys150ArgfsTer17
NM_001352607.1:c.371_372del NP_001339536.1:p.Lys124ArgfsTer17
NM_001352608.1:c.371_372del NP_001339537.1:p.Lys124ArgfsTer17
NM_001352609.1:c.449_450del NP_001339538.1:p.Lys150ArgfsTer17
NM_001352610.1:c.-418_-417del NP_001339539.1:n.-418_-417del
NM_001352611.1:c.-418_-417del NP_001339540.1:n.-418_-417del
NM_001352612.1:c.-418_-417del NP_001339541.1:n.-418_-417del
NR_148027.1:n.555_556del
NR_148028.1:n.555_556del
NR_148029.1:n.477_478del
NR_148030.1:n.555_556del
NR_148031.1:n.555_556del
XM_017020605.1:c.449_450del XP_016876094.1:p.Lys150ArgfsTer17
XM_017020606.1:c.371_372del XP_016876095.1:p.Lys124ArgfsTer17
XM_017020607.1:c.350_351del XP_016876096.1:p.Lys117ArgfsTer17
XM_017020609.1:c.350_351del XP_016876098.1:p.Lys117ArgfsTer17
XM_017020611.1:c.449_450del XP_016876100.1:p.Lys150ArgfsTer17
XM_017020612.1:c.449_450del XP_016876101.1:p.Lys150ArgfsTer17
XM_017020613.1:c.449_450del XP_016876102.1:p.Lys150ArgfsTer17
XM_017020615.1:c.449_450del XP_016876104.1:p.Lys150ArgfsTer17
XM_017020616.1:c.449_450del XP_016876105.1:p.Lys150ArgfsTer17
XR_001749567.1:n.550_551del
XR_001749568.1:n.550_551del
XR_001749569.1:n.550_551del
XR_001749574.1:n.401_402del
XR_001749576.1:n.550_551del
XR_001749577.1:n.550_551del
NM_000282.4:c.449_450del MANE Select NP_000273.2:p.Lys150ArgfsTer17
NM_001352605.2:c.449_450del NP_001339534.1:p.Lys150ArgfsTer17
NM_001352606.2:c.449_450del NP_001339535.1:p.Lys150ArgfsTer17
NM_001352607.2:c.371_372del NP_001339536.1:p.Lys124ArgfsTer17
NM_001352608.2:c.371_372del NP_001339537.1:p.Lys124ArgfsTer17
NM_001352609.2:c.449_450del NP_001339538.1:p.Lys150ArgfsTer17
NM_001352610.2:c.-418_-417del NP_001339539.1:n.-418_-417del
NM_001352611.2:c.-418_-417del NP_001339540.1:n.-418_-417del
NM_001352612.2:c.-418_-417del NP_001339541.1:n.-418_-417del
NR_148027.2:n.477_478del
NR_148028.2:n.477_478del
NR_148029.2:n.399_400del
NR_148030.2:n.477_478del
NR_148031.2:n.477_478del
NM_001127692.3:c.371_372del NP_001121164.1:p.Lys124ArgfsTer17
NM_001178004.2:c.449_450del NP_001171475.1:p.Lys150ArgfsTer17