Canonical Allele Identifier: CA1942335648
Gene: OAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124397985C= , CM000672.2:g.124397985C= GRCh38
NC_000010.10:g.126086554C= , CM000672.1:g.126086554C= GRCh37
NC_000010.9:g.126076544C= NCBI36
NG_008861.1:g.25966G= , LRG_685:g.25966G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368845.6:c.1277G= MANE Select ENSP00000357838.5:p.Arg426=
ENST00000368845.5:c.1277G= ENSP00000357838.5:p.Arg426=
ENST00000539214.5:c.863G= ENSP00000439042.1:p.Arg288=
NM_000274.3:c.1277G= , LRG_685t1:c.1277G= NP_000265.1:p.Arg426=
NM_001171814.1:c.863G= NP_001165285.1:p.Arg288=
XM_006717871.2:c.1277G= XP_006717934.1:p.Arg426=
XM_011539833.1:c.1277G= XP_011538135.1:p.Arg426=
XM_011539834.1:c.1277G= XP_011538136.1:p.Arg426=
NM_001322965.1:c.1277G= NP_001309894.1:p.Arg426=
NM_001322966.1:c.1277G= NP_001309895.1:p.Arg426=
NM_001322967.1:c.1277G= NP_001309896.1:p.Arg426=
NM_001322968.1:c.1277G= NP_001309897.1:p.Arg426=
NM_001322969.1:c.1277G= NP_001309898.1:p.Arg426=
NM_001322970.1:c.1277G= NP_001309899.1:p.Arg426=
NM_001322971.1:c.956G= NP_001309900.1:p.Arg319=
NM_001322974.1:c.677G= NP_001309903.1:p.Arg226=
XM_017016279.1:c.677G= XP_016871768.1:p.Arg226=
NM_000274.4:c.1277G= MANE Select NP_000265.1:p.Arg426=
NM_001322965.2:c.1277G= NP_001309894.1:p.Arg426=
NM_001322966.2:c.1277G= NP_001309895.1:p.Arg426=
NM_001322967.2:c.1277G= NP_001309896.1:p.Arg426=
NM_001322968.2:c.1277G= NP_001309897.1:p.Arg426=
NM_001322969.2:c.1277G= NP_001309898.1:p.Arg426=
NM_001322970.2:c.1277G= NP_001309899.1:p.Arg426=
NM_001322971.2:c.956G= NP_001309900.1:p.Arg319=
NM_001322974.2:c.677G= NP_001309903.1:p.Arg226=
NM_001171814.2:c.863G= NP_001165285.1:p.Arg288=