Canonical Allele Identifier: CA611991303
Gene: PCCA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100103147_100103148del , CM000675.2:g.100103147_100103148del GRCh38
NC_000013.10:g.100755401_100755402del , CM000675.1:g.100755401_100755402del GRCh37
NC_000013.9:g.99553402_99553403del NCBI36
NG_008768.1:g.19065_19066del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376285.6:c.183+187_183+188del MANE Select ENSP00000365462.1:n.183+187_183+188del
ENST00000636366.1:c.62+187_62+188del
ENST00000636420.1:c.62+187_62+188del
ENST00000636475.1:c.62+187_62+188del
ENST00000637358.1:c.62+187_62+188del
ENST00000637657.1:c.62+187_62+188del
ENST00000647303.1:c.183+187_183+188del ENSP00000495663.1:n.183+187_183+188del
ENST00000376279.7:c.183+187_183+188del ENSP00000365456.3:n.183+187_183+188del
ENST00000376285.5:c.183+187_183+188del ENSP00000365462.1:n.183+187_183+188del
ENST00000376286.8:c.106-8694_106-8693del ENSP00000365463.4:n.106-8694_106-8693del
NM_000282.3:c.183+187_183+188del NP_000273.2:n.183+187_183+188del
NM_001127692.2:c.106-8694_106-8693del NP_001121164.1:n.106-8694_106-8693del
NM_001178004.1:c.183+187_183+188del NP_001171475.1:n.183+187_183+188del
XM_005254059.2:c.183+187_183+188del XP_005254116.1:n.183+187_183+188del
XM_011521093.1:c.183+187_183+188del XP_011519395.1:n.183+187_183+188del
XR_931615.1:n.284+187_284+188del
XR_931616.1:n.284+187_284+188del
NM_001352605.1:c.183+187_183+188del NP_001339534.1:n.183+187_183+188del
NM_001352606.1:c.183+187_183+188del NP_001339535.1:n.183+187_183+188del
NM_001352607.1:c.106-8694_106-8693del NP_001339536.1:n.106-8694_106-8693del
NM_001352608.1:c.106-8694_106-8693del NP_001339537.1:n.106-8694_106-8693del
NM_001352609.1:c.183+187_183+188del NP_001339538.1:n.183+187_183+188del
NM_001352610.1:c.-684+187_-684+188del NP_001339539.1:n.-684+187_-684+188del
NM_001352611.1:c.-684+187_-684+188del NP_001339540.1:n.-684+187_-684+188del
NM_001352612.1:c.-684+187_-684+188del NP_001339541.1:n.-684+187_-684+188del
NR_148027.1:n.289+187_289+188del
NR_148028.1:n.289+187_289+188del
NR_148029.1:n.212-8694_212-8693del
NR_148030.1:n.289+187_289+188del
NR_148031.1:n.289+187_289+188del
XM_017020605.1:c.183+187_183+188del XP_016876094.1:n.183+187_183+188del
XM_017020606.1:c.106-8694_106-8693del XP_016876095.1:n.106-8694_106-8693del
XM_017020607.1:c.84+187_84+188del XP_016876096.1:n.84+187_84+188del
XM_017020609.1:c.84+187_84+188del XP_016876098.1:n.84+187_84+188del
XM_017020611.1:c.183+187_183+188del XP_016876100.1:n.183+187_183+188del
XM_017020612.1:c.183+187_183+188del XP_016876101.1:n.183+187_183+188del
XM_017020613.1:c.183+187_183+188del XP_016876102.1:n.183+187_183+188del
XM_017020615.1:c.183+187_183+188del XP_016876104.1:n.183+187_183+188del
XM_017020616.1:c.183+187_183+188del XP_016876105.1:n.183+187_183+188del
XR_001749567.1:n.284+187_284+188del
XR_001749568.1:n.284+187_284+188del
XR_001749569.1:n.284+187_284+188del
XR_001749574.1:n.136-8694_136-8693del
XR_001749576.1:n.284+187_284+188del
XR_001749577.1:n.284+187_284+188del
NM_000282.4:c.183+187_183+188del MANE Select NP_000273.2:n.183+187_183+188del
NM_001352605.2:c.183+187_183+188del NP_001339534.1:n.183+187_183+188del
NM_001352606.2:c.183+187_183+188del NP_001339535.1:n.183+187_183+188del
NM_001352607.2:c.106-8694_106-8693del NP_001339536.1:n.106-8694_106-8693del
NM_001352608.2:c.106-8694_106-8693del NP_001339537.1:n.106-8694_106-8693del
NM_001352609.2:c.183+187_183+188del NP_001339538.1:n.183+187_183+188del
NM_001352610.2:c.-684+187_-684+188del NP_001339539.1:n.-684+187_-684+188del
NM_001352611.2:c.-684+187_-684+188del NP_001339540.1:n.-684+187_-684+188del
NM_001352612.2:c.-684+187_-684+188del NP_001339541.1:n.-684+187_-684+188del
NR_148027.2:n.211+187_211+188del
NR_148028.2:n.211+187_211+188del
NR_148029.2:n.134-8694_134-8693del
NR_148030.2:n.211+187_211+188del
NR_148031.2:n.211+187_211+188del
NM_001127692.3:c.106-8694_106-8693del NP_001121164.1:n.106-8694_106-8693del
NM_001178004.2:c.183+187_183+188del NP_001171475.1:n.183+187_183+188del