Canonical Allele Identifier: CA2114011366
Gene: PCCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100268719T= , CM000675.2:g.100268719T= GRCh38
NC_000013.10:g.100920973T= , CM000675.1:g.100920973T= GRCh37
NC_000013.9:g.99718974T= NCBI36
NG_008768.1:g.184637T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376285.6:c.850T= MANE Select ENSP00000365462.1:p.Trp284=
ENST00000636366.1:c.729T=
ENST00000636420.1:c.729T=
ENST00000636475.1:c.729T=
ENST00000637657.1:c.729T=
ENST00000647303.1:c.*698T= ENSP00000495663.1:n.*698T=
ENST00000376279.7:c.850T= ENSP00000365456.3:p.Trp284=
ENST00000376285.5:c.850T= ENSP00000365462.1:p.Trp284=
ENST00000376286.8:c.772T= ENSP00000365463.4:p.Trp258=
NM_000282.3:c.850T= NP_000273.2:p.Trp284=
NM_001127692.2:c.772T= NP_001121164.1:p.Trp258=
NM_001178004.1:c.850T= NP_001171475.1:p.Trp284=
XM_005254059.2:c.850T= XP_005254116.1:p.Trp284=
XM_011521093.1:c.850T= XP_011519395.1:p.Trp284=
XR_931615.1:n.951T=
XR_931616.1:n.951T=
NM_001352605.1:c.850T= NP_001339534.1:p.Trp284=
NM_001352606.1:c.850T= NP_001339535.1:p.Trp284=
NM_001352607.1:c.772T= NP_001339536.1:p.Trp258=
NM_001352608.1:c.772T= NP_001339537.1:p.Trp258=
NM_001352609.1:c.850T= NP_001339538.1:p.Trp284=
NM_001352610.1:c.-96T= NP_001339539.1:n.-96T=
NM_001352611.1:c.-96T= NP_001339540.1:n.-96T=
NM_001352612.1:c.-96T= NP_001339541.1:n.-96T=
NR_148027.1:n.956T=
NR_148028.1:n.956T=
NR_148029.1:n.878T=
NR_148030.1:n.956T=
NR_148031.1:n.956T=
XM_017020605.1:c.850T= XP_016876094.1:p.Trp284=
XM_017020606.1:c.772T= XP_016876095.1:p.Trp258=
XM_017020607.1:c.751T= XP_016876096.1:p.Trp251=
XM_017020609.1:c.751T= XP_016876098.1:p.Trp251=
XM_017020611.1:c.850T= XP_016876100.1:p.Trp284=
XM_017020612.1:c.850T= XP_016876101.1:p.Trp284=
XM_017020613.1:c.850T= XP_016876102.1:p.Trp284=
XM_017020615.1:c.850T= XP_016876104.1:p.Trp284=
XM_017020616.1:c.850T= XP_016876105.1:p.Trp284=
XR_001749567.1:n.951T=
XR_001749568.1:n.951T=
XR_001749569.1:n.951T=
XR_001749574.1:n.802T=
XR_001749576.1:n.951T=
XR_001749577.1:n.951T=
NM_000282.4:c.850T= MANE Select NP_000273.2:p.Trp284=
NM_001352605.2:c.850T= NP_001339534.1:p.Trp284=
NM_001352606.2:c.850T= NP_001339535.1:p.Trp284=
NM_001352607.2:c.772T= NP_001339536.1:p.Trp258=
NM_001352608.2:c.772T= NP_001339537.1:p.Trp258=
NM_001352609.2:c.850T= NP_001339538.1:p.Trp284=
NM_001352610.2:c.-96T= NP_001339539.1:n.-96T=
NM_001352611.2:c.-96T= NP_001339540.1:n.-96T=
NM_001352612.2:c.-96T= NP_001339541.1:n.-96T=
NR_148027.2:n.878T=
NR_148028.2:n.878T=
NR_148029.2:n.800T=
NR_148030.2:n.878T=
NR_148031.2:n.878T=
NM_001127692.3:c.772T= NP_001121164.1:p.Trp258=
NM_001178004.2:c.850T= NP_001171475.1:p.Trp284=