Canonical Allele Identifier: CA5733327
Gene: OAT HGNC NCBI

Linked Data

dbSNP Id: rs767965207

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124400880del , CM000672.2:g.124400880del GRCh38
NC_000010.10:g.126089449del , CM000672.1:g.126089449del GRCh37
NC_000010.9:g.126079439del NCBI36
NG_008861.1:g.23074del , LRG_685:g.23074del

Transcript Alleles

HGVS Amino-acid change
ENST00000368845.6:c.1122del MANE Select ENSP00000357838.5:p.Gly375AspfsTer3
ENST00000368845.5:c.1122del ENSP00000357838.5:p.Gly375AspfsTer3
ENST00000471127.1:n.632del
ENST00000539214.5:c.708del ENSP00000439042.1:p.Gly237AspfsTer3
NM_000274.3:c.1122del , LRG_685t1:c.1122del NP_000265.1:p.Gly375AspfsTer3
NM_001171814.1:c.708del NP_001165285.1:p.Gly237AspfsTer3
XM_006717871.2:c.1122del XP_006717934.1:p.Gly375AspfsTer3
XM_011539833.1:c.1122del XP_011538135.1:p.Gly375AspfsTer3
XM_011539834.1:c.1122del XP_011538136.1:p.Gly375AspfsTer3
NM_001322965.1:c.1122del NP_001309894.1:p.Gly375AspfsTer3
NM_001322966.1:c.1122del NP_001309895.1:p.Gly375AspfsTer3
NM_001322967.1:c.1122del NP_001309896.1:p.Gly375AspfsTer3
NM_001322968.1:c.1122del NP_001309897.1:p.Gly375AspfsTer3
NM_001322969.1:c.1122del NP_001309898.1:p.Gly375AspfsTer3
NM_001322970.1:c.1122del NP_001309899.1:p.Gly375AspfsTer3
NM_001322971.1:c.801del NP_001309900.1:p.Gly268AspfsTer3
NM_001322974.1:c.522del NP_001309903.1:p.Gly175AspfsTer3
XM_017016279.1:c.522del XP_016871768.1:p.Gly175AspfsTer3
NM_000274.4:c.1122del MANE Select NP_000265.1:p.Gly375AspfsTer3
NM_001322965.2:c.1122del NP_001309894.1:p.Gly375AspfsTer3
NM_001322966.2:c.1122del NP_001309895.1:p.Gly375AspfsTer3
NM_001322967.2:c.1122del NP_001309896.1:p.Gly375AspfsTer3
NM_001322968.2:c.1122del NP_001309897.1:p.Gly375AspfsTer3
NM_001322969.2:c.1122del NP_001309898.1:p.Gly375AspfsTer3
NM_001322970.2:c.1122del NP_001309899.1:p.Gly375AspfsTer3
NM_001322971.2:c.801del NP_001309900.1:p.Gly268AspfsTer3
NM_001322974.2:c.522del NP_001309903.1:p.Gly175AspfsTer3
NM_001171814.2:c.708del NP_001165285.1:p.Gly237AspfsTer3