Canonical Allele Identifier: CA16609231
Gene: PREPL HGNC NCBI

Linked Data

ClinVar Variation Id: 390242
ClinVar RCV Id: RCV000437878
dbSNP Id: rs1057523690

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.44339310del , CM000664.2:g.44339310del GRCh38
NC_000002.11:g.44566449del , CM000664.1:g.44566449del GRCh37
NC_000002.10:g.44419953del NCBI36
NG_016429.1:g.27554del

Transcript Alleles

HGVS Amino-acid change
ENST00000409411.6:c.540del MANE Select ENSP00000387095.2:p.Met181Ter
ENST00000260648.10:c.807del ENSP00000260648.6:p.Met270Ter
ENST00000378511.7:c.807del ENSP00000367772.3:p.Met270Ter
ENST00000378520.7:c.807del ENSP00000367781.3:p.Met270Ter
ENST00000409272.5:c.807del ENSP00000386909.1:p.Met270Ter
ENST00000409411.5:c.540del ENSP00000387095.1:p.Met181Ter
ENST00000409936.5:c.807del ENSP00000386543.1:p.Met270Ter
ENST00000409957.5:c.540del ENSP00000387241.1:p.Met181Ter
ENST00000410081.5:c.807del ENSP00000386509.1:p.Met270Ter
ENST00000425263.5:c.807del ENSP00000391456.1:p.Met270Ter
ENST00000426481.5:c.807del ENSP00000409480.1:p.Met270Ter
ENST00000541738.5:c.540del ENSP00000439626.1:p.Met181Ter
NM_001042385.2:c.807del NP_001035844.1:p.Met270Ter
NM_001042386.2:c.807del NP_001035845.1:p.Met270Ter
NM_001171603.1:c.807del NP_001165074.1:p.Met270Ter
NM_001171606.1:c.807del NP_001165077.1:p.Met270Ter
NM_001171613.1:c.540del NP_001165084.1:p.Met181Ter
NM_001171617.1:c.540del NP_001165088.1:p.Met181Ter
NM_006036.4:c.807del NP_006027.2:p.Met270Ter
XM_011533198.1:c.807del XP_011531500.1:p.Met270Ter
XM_011533199.1:c.807del XP_011531501.1:p.Met270Ter
XM_011533200.1:c.807del XP_011531502.1:p.Met270Ter
XM_011533201.1:c.807del XP_011531503.1:p.Met270Ter
XM_011533202.1:c.540del XP_011531504.1:p.Met181Ter
XM_011533198.2:c.807del XP_011531500.1:p.Met270Ter
XM_017005384.1:c.807del XP_016860873.1:p.Met270Ter
XM_017005385.1:c.807del XP_016860874.1:p.Met270Ter
NM_001171613.2:c.540del MANE Select NP_001165084.1:p.Met181Ter
NM_001374275.1:c.807del NP_001361204.1:p.Met270Ter
NM_001374276.1:c.807del NP_001361205.1:p.Met270Ter
NM_001374277.1:c.540del NP_001361206.1:p.Met181Ter
NM_001171606.2:c.807del NP_001165077.1:p.Met270Ter