Canonical Allele Identifier: CA2114056782
Gene: PCCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100368428A= , CM000675.2:g.100368428A= GRCh38
NC_000013.10:g.101020682A= , CM000675.1:g.101020682A= GRCh37
NC_000013.9:g.99818683A= NCBI36
NG_008768.1:g.284346A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376285.6:c.1644-44A= MANE Select ENSP00000365462.1:n.1644-44A=
ENST00000636366.1:c.945-57205A=
ENST00000636475.1:c.1159-44A=
ENST00000637657.1:c.1304-44A=
ENST00000647303.1:c.*1128-44A= ENSP00000495663.1:n.*1128-44A=
ENST00000376279.7:c.1644-44A= ENSP00000365456.3:n.1644-44A=
ENST00000376285.5:c.1644-44A= ENSP00000365462.1:n.1644-44A=
ENST00000376286.8:c.1566-44A= ENSP00000365463.4:n.1566-44A=
ENST00000424527.5:c.246-44A= ENSP00000396050.1:n.246-44A=
NM_000282.3:c.1644-44A= NP_000273.2:n.1644-44A=
NM_001127692.2:c.1566-44A= NP_001121164.1:n.1566-44A=
NM_001178004.1:c.1644-44A= NP_001171475.1:n.1644-44A=
XM_005254059.2:c.1644-44A= XP_005254116.1:n.1644-44A=
XM_011521093.1:c.1644-44A= XP_011519395.1:n.1644-44A=
XR_931615.1:n.1744+28169A=
NM_001352605.1:c.1644-44A= NP_001339534.1:n.1644-44A=
NM_001352606.1:c.1500-44A= NP_001339535.1:n.1500-44A=
NM_001352607.1:c.1566-44A= NP_001339536.1:n.1566-44A=
NM_001352608.1:c.1422-44A= NP_001339537.1:n.1422-44A=
NM_001352609.1:c.1644-44A= NP_001339538.1:n.1644-44A=
NM_001352610.1:c.699-44A= NP_001339539.1:n.699-44A=
NM_001352611.1:c.699-44A= NP_001339540.1:n.699-44A=
NM_001352612.1:c.555-44A= NP_001339541.1:n.555-44A=
NR_148027.1:n.1834-44A=
NR_148028.1:n.1833+28169A=
NR_148029.1:n.1755+28169A=
NR_148030.1:n.1834-44A=
NR_148031.1:n.1749+28169A=
XM_017020605.1:c.1644-44A= XP_016876094.1:n.1644-44A=
XM_017020606.1:c.1566-44A= XP_016876095.1:n.1566-44A=
XM_017020607.1:c.1545-44A= XP_016876096.1:n.1545-44A=
XM_017020609.1:c.1545-44A= XP_016876098.1:n.1545-44A=
XM_017020611.1:c.1644-44A= XP_016876100.1:n.1644-44A=
XM_017020612.1:c.1644-44A= XP_016876101.1:n.1644-44A=
XM_017020613.1:c.1644-44A= XP_016876102.1:n.1644-44A=
XM_017020615.1:c.1644-44A= XP_016876104.1:n.1644-44A=
XR_001749567.1:n.1745-44A=
XR_001749568.1:n.1745-44A=
XR_001749569.1:n.1745-44A=
XR_001749574.1:n.1680-44A=
XR_001749576.1:n.1381-44A=
XR_001749577.1:n.1380+28169A=
NM_000282.4:c.1644-44A= MANE Select NP_000273.2:n.1644-44A=
NM_001352605.2:c.1644-44A= NP_001339534.1:n.1644-44A=
NM_001352606.2:c.1500-44A= NP_001339535.1:n.1500-44A=
NM_001352607.2:c.1566-44A= NP_001339536.1:n.1566-44A=
NM_001352608.2:c.1422-44A= NP_001339537.1:n.1422-44A=
NM_001352609.2:c.1644-44A= NP_001339538.1:n.1644-44A=
NM_001352610.2:c.699-44A= NP_001339539.1:n.699-44A=
NM_001352611.2:c.699-44A= NP_001339540.1:n.699-44A=
NM_001352612.2:c.555-44A= NP_001339541.1:n.555-44A=
NR_148027.2:n.1756-44A=
NR_148028.2:n.1755+28169A=
NR_148029.2:n.1677+28169A=
NR_148030.2:n.1756-44A=
NR_148031.2:n.1671+28169A=
NM_001127692.3:c.1566-44A= NP_001121164.1:n.1566-44A=
NM_001178004.2:c.1644-44A= NP_001171475.1:n.1644-44A=