Canonical Allele Identifier: CA383735532
Community Standard Title: NM_001351132.2(PEX5):c.1512T>G (p.Tyr504Ter)
Gene: PEX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.7209122T>G , CM000674.2:g.7209122T>G GRCh38
NC_000012.11:g.7361718T>G , CM000674.1:g.7361718T>G GRCh37
NC_000012.10:g.7252985T>G NCBI36
NG_008448.1:g.24960T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001351132.2:c.1512T>G MANE Select NP_001338061.1:p.Tyr504Ter
ENST00000675855.1:c.1512T>G MANE Select ENSP00000502374.1:p.Tyr504Ter
NM_000319.4:c.1488T>G NP_000310.2:p.Tyr496Ter
NM_000319.5:c.1488T>G NP_000310.2:p.Tyr496Ter
NM_001131023.1:c.1557T>G NP_001124495.1:p.Tyr519Ter
NM_001131023.2:c.1557T>G NP_001124495.1:p.Tyr519Ter
NM_001131024.1:c.1401T>G NP_001124496.1:p.Tyr467Ter
NM_001131024.2:c.1401T>G NP_001124496.1:p.Tyr467Ter
NM_001131025.1:c.1512T>G NP_001124497.1:p.Tyr504Ter
NM_001131025.2:c.1512T>G NP_001124497.1:p.Tyr504Ter
NM_001131026.1:c.1512T>G NP_001124498.1:p.Tyr504Ter
NM_001131026.2:c.1512T>G NP_001124498.1:p.Tyr504Ter
NM_001300789.1:c.1575T>G NP_001287718.1:p.Tyr525Ter
NM_001300789.3:c.1512T>G NP_001287718.2:p.Tyr504Ter
NM_001351124.1:c.1401T>G NP_001338053.1:p.Tyr467Ter
NM_001351124.3:c.1401T>G NP_001338053.1:p.Tyr467Ter
NM_001351126.1:c.1401T>G NP_001338055.1:p.Tyr467Ter
NM_001351126.2:c.1401T>G NP_001338055.1:p.Tyr467Ter
NM_001351127.1:c.1401T>G NP_001338056.1:p.Tyr467Ter
NM_001351127.2:c.1401T>G NP_001338056.1:p.Tyr467Ter
NM_001351128.1:c.1401T>G NP_001338057.1:p.Tyr467Ter
NM_001351128.2:c.1401T>G NP_001338057.1:p.Tyr467Ter
NM_001351130.1:c.1401T>G NP_001338059.1:p.Tyr467Ter
NM_001351130.3:c.1401T>G NP_001338059.1:p.Tyr467Ter
NM_001351131.1:c.1512T>G NP_001338060.1:p.Tyr504Ter
NM_001351131.2:c.1512T>G NP_001338060.1:p.Tyr504Ter
NM_001351132.1:c.1512T>G NP_001338061.1:p.Tyr504Ter
NM_001351133.1:c.1512T>G NP_001338062.1:p.Tyr504Ter
NM_001351133.2:c.1512T>G NP_001338062.1:p.Tyr504Ter
NM_001351134.1:c.1512T>G NP_001338063.1:p.Tyr504Ter
NM_001351134.2:c.1512T>G NP_001338063.1:p.Tyr504Ter
NM_001351135.1:c.1509T>G NP_001338064.1:p.Tyr503Ter
NM_001351135.3:c.1446T>G NP_001338064.2:p.Tyr482Ter
NM_001351136.1:c.1503T>G NP_001338065.1:p.Tyr501Ter
NM_001351136.2:c.1503T>G NP_001338065.1:p.Tyr501Ter
NM_001351137.1:c.1464T>G NP_001338066.1:p.Tyr488Ter
NM_001351137.3:c.1401T>G NP_001338066.2:p.Tyr467Ter
NM_001351138.1:c.1446T>G NP_001338067.1:p.Tyr482Ter
NM_001351138.2:c.1446T>G NP_001338067.1:p.Tyr482Ter
NM_001351139.1:c.1377T>G NP_001338068.1:p.Tyr459Ter
NM_001351139.2:c.1377T>G NP_001338068.1:p.Tyr459Ter
NM_001351140.1:c.1377T>G NP_001338069.1:p.Tyr459Ter
NM_001351140.2:c.1377T>G NP_001338069.1:p.Tyr459Ter
NM_001374645.1:c.1401T>G NP_001361574.1:p.Tyr467Ter
NM_001374646.1:c.1401T>G NP_001361575.1:p.Tyr467Ter
NM_001374647.2:c.1512T>G NP_001361576.1:p.Tyr504Ter
NM_001374648.2:c.1401T>G NP_001361577.1:p.Tyr467Ter
NM_001374649.2:c.1377T>G NP_001361578.1:p.Tyr459Ter
ENST00000266563.9:c.1401T>G ENSP00000266563.5:p.Tyr467Ter
ENST00000266564.7:c.1488T>G ENSP00000266564.3:p.Tyr496Ter
ENST00000412720.6:c.1575T>G ENSP00000391601.2:p.Tyr525Ter
ENST00000420616.6:c.1512T>G ENSP00000410159.2:p.Tyr504Ter
ENST00000434354.6:c.1557T>G ENSP00000407401.2:p.Tyr519Ter
ENST00000455147.6:c.1512T>G ENSP00000400647.2:p.Tyr504Ter
XM_005253455.1:c.1464T>G XP_005253512.1:p.Tyr488Ter
XM_011520793.1:c.1620T>G XP_011519095.1:p.Tyr540Ter
XM_011520793.2:c.1620T>G XP_011519095.1:p.Tyr540Ter
XM_011520794.1:c.1620T>G XP_011519096.1:p.Tyr540Ter
XM_011520795.1:c.1557T>G XP_011519097.1:p.Tyr519Ter
XM_011520796.1:c.1557T>G XP_011519098.1:p.Tyr519Ter
XM_011520797.1:c.1512T>G XP_011519099.1:p.Tyr504Ter
XM_011520798.1:c.1512T>G XP_011519100.1:p.Tyr504Ter
XM_011520799.1:c.1512T>G XP_011519101.1:p.Tyr504Ter
XM_011520800.1:c.1512T>G XP_011519102.1:p.Tyr504Ter
XM_011520801.1:c.1509T>G XP_011519103.1:p.Tyr503Ter
XM_011520802.1:c.1263T>G XP_011519104.1:p.Tyr421Ter
XM_011520802.2:c.1263T>G XP_011519104.1:p.Tyr421Ter
XM_017019744.1:c.1956T>G XP_016875233.1:p.Tyr652Ter
XM_017019745.1:c.1956T>G XP_016875234.1:p.Tyr652Ter
XM_017019746.1:c.1845T>G XP_016875235.1:p.Tyr615Ter
XM_017019747.1:c.1821T>G XP_016875236.1:p.Tyr607Ter
XM_017019748.1:c.1557T>G XP_016875237.1:p.Tyr519Ter
XM_017019749.1:c.1512T>G XP_016875238.1:p.Tyr504Ter
XM_017019750.1:c.1488T>G XP_016875239.1:p.Tyr496Ter
XR_001748833.1:n.1998T>G