Canonical Allele Identifier: CA144133
Gene: OAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124400971del , CM000672.2:g.124400971del GRCh38
NC_000010.10:g.126089540del , CM000672.1:g.126089540del GRCh37
NC_000010.9:g.126079530del NCBI36
NG_008861.1:g.22983del , LRG_685:g.22983del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.1031del MANE Select ENSP00000357838.5:p.Asn344ThrfsTer13
ENST00000368845.5:c.1031del ENSP00000357838.5:p.Asn344ThrfsTer13
ENST00000471127.1:n.541del
ENST00000539214.5:c.617del ENSP00000439042.1:p.Asn206ThrfsTer13
NM_000274.3:c.1031del , LRG_685t1:c.1031del NP_000265.1:p.Asn344ThrfsTer13
NM_001171814.1:c.617del NP_001165285.1:p.Asn206ThrfsTer13
XM_006717871.2:c.1031del XP_006717934.1:p.Asn344ThrfsTer13
XM_011539833.1:c.1031del XP_011538135.1:p.Asn344ThrfsTer13
XM_011539834.1:c.1031del XP_011538136.1:p.Asn344ThrfsTer13
NM_001322965.1:c.1031del NP_001309894.1:p.Asn344ThrfsTer13
NM_001322966.1:c.1031del NP_001309895.1:p.Asn344ThrfsTer13
NM_001322967.1:c.1031del NP_001309896.1:p.Asn344ThrfsTer13
NM_001322968.1:c.1031del NP_001309897.1:p.Asn344ThrfsTer13
NM_001322969.1:c.1031del NP_001309898.1:p.Asn344ThrfsTer13
NM_001322970.1:c.1031del NP_001309899.1:p.Asn344ThrfsTer13
NM_001322971.1:c.710del NP_001309900.1:p.Asn237ThrfsTer13
NM_001322974.1:c.431del NP_001309903.1:p.Asn144ThrfsTer13
XM_017016279.1:c.431del XP_016871768.1:p.Asn144ThrfsTer13
NM_000274.4:c.1031del MANE Select NP_000265.1:p.Asn344ThrfsTer13
NM_001322965.2:c.1031del NP_001309894.1:p.Asn344ThrfsTer13
NM_001322966.2:c.1031del NP_001309895.1:p.Asn344ThrfsTer13
NM_001322967.2:c.1031del NP_001309896.1:p.Asn344ThrfsTer13
NM_001322968.2:c.1031del NP_001309897.1:p.Asn344ThrfsTer13
NM_001322969.2:c.1031del NP_001309898.1:p.Asn344ThrfsTer13
NM_001322970.2:c.1031del NP_001309899.1:p.Asn344ThrfsTer13
NM_001322971.2:c.710del NP_001309900.1:p.Asn237ThrfsTer13
NM_001322974.2:c.431del NP_001309903.1:p.Asn144ThrfsTer13
NM_001171814.2:c.617del NP_001165285.1:p.Asn206ThrfsTer13