Canonical Allele Identifier: CA612004519
Gene: PCCA HGNC NCBI

Linked Data

dbSNP Id: rs146754385

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100309801_100309806dup , CM000675.2:g.100309801_100309806dup GRCh38
NC_000013.10:g.100962055_100962060dup , CM000675.1:g.100962055_100962060dup GRCh37
NC_000013.9:g.99760056_99760061dup NCBI36
NG_008768.1:g.225719_225724dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376285.6:c.1354-32_1354-27dup MANE Select ENSP00000365462.1:n.1354-32_1354-27dup
ENST00000636366.1:c.944+36455_944+36460dup
ENST00000636420.1:c.1231-32_1231-27dup
ENST00000636475.1:c.945-20760_945-20755dup
ENST00000637657.1:c.1014-32_1014-27dup
ENST00000647303.1:c.*914-20760_*914-20755dup ENSP00000495663.1:n.*914-20760_*914-20755dup
ENST00000376279.7:c.1354-32_1354-27dup ENSP00000365456.3:n.1354-32_1354-27dup
ENST00000376285.5:c.1354-32_1354-27dup ENSP00000365462.1:n.1354-32_1354-27dup
ENST00000376286.8:c.1276-32_1276-27dup ENSP00000365463.4:n.1276-32_1276-27dup
ENST00000424527.5:c.31+16547_31+16552dup ENSP00000396050.1:n.31+16547_31+16552dup
ENST00000443601.1:c.129-32_129-27dup
NM_000282.3:c.1354-32_1354-27dup NP_000273.2:n.1354-32_1354-27dup
NM_001127692.2:c.1276-32_1276-27dup NP_001121164.1:n.1276-32_1276-27dup
NM_001178004.1:c.1354-32_1354-27dup NP_001171475.1:n.1354-32_1354-27dup
XM_005254059.2:c.1354-32_1354-27dup XP_005254116.1:n.1354-32_1354-27dup
XM_011521093.1:c.1354-32_1354-27dup XP_011519395.1:n.1354-32_1354-27dup
XR_931615.1:n.1455-32_1455-27dup
NM_001352605.1:c.1354-32_1354-27dup NP_001339534.1:n.1354-32_1354-27dup
NM_001352606.1:c.1210-32_1210-27dup NP_001339535.1:n.1210-32_1210-27dup
NM_001352607.1:c.1276-32_1276-27dup NP_001339536.1:n.1276-32_1276-27dup
NM_001352608.1:c.1132-32_1132-27dup NP_001339537.1:n.1132-32_1132-27dup
NM_001352609.1:c.1354-32_1354-27dup NP_001339538.1:n.1354-32_1354-27dup
NM_001352610.1:c.409-32_409-27dup NP_001339539.1:n.409-32_409-27dup
NM_001352611.1:c.409-32_409-27dup NP_001339540.1:n.409-32_409-27dup
NM_001352612.1:c.265-32_265-27dup NP_001339541.1:n.265-32_265-27dup
NR_148027.1:n.1544-32_1544-27dup
NR_148028.1:n.1544-32_1544-27dup
NR_148029.1:n.1466-32_1466-27dup
NR_148030.1:n.1544-32_1544-27dup
NR_148031.1:n.1460-32_1460-27dup
XM_017020605.1:c.1354-32_1354-27dup XP_016876094.1:n.1354-32_1354-27dup
XM_017020606.1:c.1276-32_1276-27dup XP_016876095.1:n.1276-32_1276-27dup
XM_017020607.1:c.1255-32_1255-27dup XP_016876096.1:n.1255-32_1255-27dup
XM_017020609.1:c.1255-32_1255-27dup XP_016876098.1:n.1255-32_1255-27dup
XM_017020611.1:c.1354-32_1354-27dup XP_016876100.1:n.1354-32_1354-27dup
XM_017020612.1:c.1354-32_1354-27dup XP_016876101.1:n.1354-32_1354-27dup
XM_017020613.1:c.1354-32_1354-27dup XP_016876102.1:n.1354-32_1354-27dup
XM_017020615.1:c.1354-32_1354-27dup XP_016876104.1:n.1354-32_1354-27dup
XM_017020616.1:c.1354-32_1354-27dup XP_016876105.1:n.1354-32_1354-27dup
XR_001749567.1:n.1455-32_1455-27dup
XR_001749568.1:n.1455-32_1455-27dup
XR_001749569.1:n.1455-32_1455-27dup
XR_001749574.1:n.1390-32_1390-27dup
XR_001749576.1:n.1167-20760_1167-20755dup
XR_001749577.1:n.1167-20760_1167-20755dup
NM_000282.4:c.1354-32_1354-27dup MANE Select NP_000273.2:n.1354-32_1354-27dup
NM_001352605.2:c.1354-32_1354-27dup NP_001339534.1:n.1354-32_1354-27dup
NM_001352606.2:c.1210-32_1210-27dup NP_001339535.1:n.1210-32_1210-27dup
NM_001352607.2:c.1276-32_1276-27dup NP_001339536.1:n.1276-32_1276-27dup
NM_001352608.2:c.1132-32_1132-27dup NP_001339537.1:n.1132-32_1132-27dup
NM_001352609.2:c.1354-32_1354-27dup NP_001339538.1:n.1354-32_1354-27dup
NM_001352610.2:c.409-32_409-27dup NP_001339539.1:n.409-32_409-27dup
NM_001352611.2:c.409-32_409-27dup NP_001339540.1:n.409-32_409-27dup
NM_001352612.2:c.265-32_265-27dup NP_001339541.1:n.265-32_265-27dup
NR_148027.2:n.1466-32_1466-27dup
NR_148028.2:n.1466-32_1466-27dup
NR_148029.2:n.1388-32_1388-27dup
NR_148030.2:n.1466-32_1466-27dup
NR_148031.2:n.1382-32_1382-27dup
NM_001127692.3:c.1276-32_1276-27dup NP_001121164.1:n.1276-32_1276-27dup
NM_001178004.2:c.1354-32_1354-27dup NP_001171475.1:n.1354-32_1354-27dup