Canonical Allele Identifier: CA2623556551

Gene: PCCA

Linked Data

• gnomAD v4: 13-100157366-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100157368del , CM000675.2:g.100157368del	GRCh38
NC_000013.10:g.100809622del , CM000675.1:g.100809622del	GRCh37
NC_000013.9:g.99607623del	NCBI36
NG_008768.1:g.73286del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376285.6:c.468+28del MANE Select	ENSP00000365462.1:n.468+28del
ENST00000636366.1:c.347+28del
ENST00000636420.1:c.347+28del
ENST00000636475.1:c.347+28del
ENST00000637358.1:c.347+28del
ENST00000637657.1:c.347+28del
ENST00000647303.1:c.*316+28del	ENSP00000495663.1:n.*316+28del
ENST00000376279.7:c.468+28del	ENSP00000365456.3:n.468+28del
ENST00000376285.5:c.468+28del	ENSP00000365462.1:n.468+28del
ENST00000376286.8:c.390+28del	ENSP00000365463.4:n.390+28del
ENST00000485946.1:n.836+28del
NM_000282.3:c.468+28del	NP_000273.2:n.468+28del
NM_001127692.2:c.390+28del	NP_001121164.1:n.390+28del
NM_001178004.1:c.468+28del	NP_001171475.1:n.468+28del
XM_005254059.2:c.468+28del	XP_005254116.1:n.468+28del
XM_011521093.1:c.468+28del	XP_011519395.1:n.468+28del
XR_931615.1:n.569+28del
XR_931616.1:n.569+28del
NM_001352605.1:c.468+28del	NP_001339534.1:n.468+28del
NM_001352606.1:c.468+28del	NP_001339535.1:n.468+28del
NM_001352607.1:c.390+28del	NP_001339536.1:n.390+28del
NM_001352608.1:c.390+28del	NP_001339537.1:n.390+28del
NM_001352609.1:c.468+28del	NP_001339538.1:n.468+28del
NM_001352610.1:c.-399+28del	NP_001339539.1:n.-399+28del
NM_001352611.1:c.-399+28del	NP_001339540.1:n.-399+28del
NM_001352612.1:c.-399+28del	NP_001339541.1:n.-399+28del
NR_148027.1:n.574+28del
NR_148028.1:n.574+28del
NR_148029.1:n.496+28del
NR_148030.1:n.574+28del
NR_148031.1:n.574+28del
XM_017020605.1:c.468+28del	XP_016876094.1:n.468+28del
XM_017020606.1:c.390+28del	XP_016876095.1:n.390+28del
XM_017020607.1:c.369+28del	XP_016876096.1:n.369+28del
XM_017020609.1:c.369+28del	XP_016876098.1:n.369+28del
XM_017020611.1:c.468+28del	XP_016876100.1:n.468+28del
XM_017020612.1:c.468+28del	XP_016876101.1:n.468+28del
XM_017020613.1:c.468+28del	XP_016876102.1:n.468+28del
XM_017020615.1:c.468+28del	XP_016876104.1:n.468+28del
XM_017020616.1:c.468+28del	XP_016876105.1:n.468+28del
XR_001749567.1:n.569+28del
XR_001749568.1:n.569+28del
XR_001749569.1:n.569+28del
XR_001749574.1:n.420+28del
XR_001749576.1:n.569+28del
XR_001749577.1:n.569+28del
NM_000282.4:c.468+28del MANE Select	NP_000273.2:n.468+28del
NM_001352605.2:c.468+28del	NP_001339534.1:n.468+28del
NM_001352606.2:c.468+28del	NP_001339535.1:n.468+28del
NM_001352607.2:c.390+28del	NP_001339536.1:n.390+28del
NM_001352608.2:c.390+28del	NP_001339537.1:n.390+28del
NM_001352609.2:c.468+28del	NP_001339538.1:n.468+28del
NM_001352610.2:c.-399+28del	NP_001339539.1:n.-399+28del
NM_001352611.2:c.-399+28del	NP_001339540.1:n.-399+28del
NM_001352612.2:c.-399+28del	NP_001339541.1:n.-399+28del
NR_148027.2:n.496+28del
NR_148028.2:n.496+28del
NR_148029.2:n.418+28del
NR_148030.2:n.496+28del
NR_148031.2:n.496+28del
NM_001127692.3:c.390+28del	NP_001121164.1:n.390+28del
NM_001178004.2:c.468+28del	NP_001171475.1:n.468+28del