Canonical Allele Identifier: CA16606386
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 381029
dbSNP Id: rs1057520932

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100157278A>G , CM000675.2:g.100157278A>G GRCh38
NC_000013.10:g.100809532A>G , CM000675.1:g.100809532A>G GRCh37
NC_000013.9:g.99607533A>G NCBI36
NG_008768.1:g.73196A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376285.6:c.415-9A>G MANE Select ENSP00000365462.1:n.415-9A>G
ENST00000636366.1:c.294-9A>G
ENST00000636420.1:c.294-9A>G
ENST00000636475.1:c.294-9A>G
ENST00000637358.1:c.294-9A>G
ENST00000637657.1:c.294-9A>G
ENST00000647303.1:c.*263-9A>G ENSP00000495663.1:n.*263-9A>G
ENST00000376279.7:c.415-9A>G ENSP00000365456.3:n.415-9A>G
ENST00000376285.5:c.415-9A>G ENSP00000365462.1:n.415-9A>G
ENST00000376286.8:c.337-9A>G ENSP00000365463.4:n.337-9A>G
ENST00000485946.1:n.783-9A>G
NM_000282.3:c.415-9A>G NP_000273.2:n.415-9A>G
NM_001127692.2:c.337-9A>G NP_001121164.1:n.337-9A>G
NM_001178004.1:c.415-9A>G NP_001171475.1:n.415-9A>G
XM_005254059.2:c.415-9A>G XP_005254116.1:n.415-9A>G
XM_011521093.1:c.415-9A>G XP_011519395.1:n.415-9A>G
XR_931615.1:n.516-9A>G
XR_931616.1:n.516-9A>G
NM_001352605.1:c.415-9A>G NP_001339534.1:n.415-9A>G
NM_001352606.1:c.415-9A>G NP_001339535.1:n.415-9A>G
NM_001352607.1:c.337-9A>G NP_001339536.1:n.337-9A>G
NM_001352608.1:c.337-9A>G NP_001339537.1:n.337-9A>G
NM_001352609.1:c.415-9A>G NP_001339538.1:n.415-9A>G
NM_001352610.1:c.-452-9A>G NP_001339539.1:n.-452-9A>G
NM_001352611.1:c.-452-9A>G NP_001339540.1:n.-452-9A>G
NM_001352612.1:c.-452-9A>G NP_001339541.1:n.-452-9A>G
NR_148027.1:n.521-9A>G
NR_148028.1:n.521-9A>G
NR_148029.1:n.443-9A>G
NR_148030.1:n.521-9A>G
NR_148031.1:n.521-9A>G
XM_017020605.1:c.415-9A>G XP_016876094.1:n.415-9A>G
XM_017020606.1:c.337-9A>G XP_016876095.1:n.337-9A>G
XM_017020607.1:c.316-9A>G XP_016876096.1:n.316-9A>G
XM_017020609.1:c.316-9A>G XP_016876098.1:n.316-9A>G
XM_017020611.1:c.415-9A>G XP_016876100.1:n.415-9A>G
XM_017020612.1:c.415-9A>G XP_016876101.1:n.415-9A>G
XM_017020613.1:c.415-9A>G XP_016876102.1:n.415-9A>G
XM_017020615.1:c.415-9A>G XP_016876104.1:n.415-9A>G
XM_017020616.1:c.415-9A>G XP_016876105.1:n.415-9A>G
XR_001749567.1:n.516-9A>G
XR_001749568.1:n.516-9A>G
XR_001749569.1:n.516-9A>G
XR_001749574.1:n.367-9A>G
XR_001749576.1:n.516-9A>G
XR_001749577.1:n.516-9A>G
NM_000282.4:c.415-9A>G MANE Select NP_000273.2:n.415-9A>G
NM_001352605.2:c.415-9A>G NP_001339534.1:n.415-9A>G
NM_001352606.2:c.415-9A>G NP_001339535.1:n.415-9A>G
NM_001352607.2:c.337-9A>G NP_001339536.1:n.337-9A>G
NM_001352608.2:c.337-9A>G NP_001339537.1:n.337-9A>G
NM_001352609.2:c.415-9A>G NP_001339538.1:n.415-9A>G
NM_001352610.2:c.-452-9A>G NP_001339539.1:n.-452-9A>G
NM_001352611.2:c.-452-9A>G NP_001339540.1:n.-452-9A>G
NM_001352612.2:c.-452-9A>G NP_001339541.1:n.-452-9A>G
NR_148027.2:n.443-9A>G
NR_148028.2:n.443-9A>G
NR_148029.2:n.365-9A>G
NR_148030.2:n.443-9A>G
NR_148031.2:n.443-9A>G
NM_001127692.3:c.337-9A>G NP_001121164.1:n.337-9A>G
NM_001178004.2:c.415-9A>G NP_001171475.1:n.415-9A>G