Canonical Allele Identifier: CA1942339019
Gene: OAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124405357A= , CM000672.2:g.124405357A= GRCh38
NC_000010.10:g.126093926A= , CM000672.1:g.126093926A= GRCh37
NC_000010.9:g.126083916A= NCBI36
NG_008861.1:g.18594T= , LRG_685:g.18594T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.648+79T= MANE Select ENSP00000357838.5:n.648+79T=
ENST00000368845.5:c.648+79T= ENSP00000357838.5:n.648+79T=
ENST00000467675.5:n.449+79T=
ENST00000483711.1:n.494+79T=
ENST00000539214.5:c.234+79T= ENSP00000439042.1:n.234+79T=
NM_000274.3:c.648+79T= , LRG_685t1:c.648+79T= NP_000265.1:n.648+79T=
NM_001171814.1:c.234+79T= NP_001165285.1:n.234+79T=
XM_006717871.2:c.648+79T= XP_006717934.1:n.648+79T=
XM_011539833.1:c.648+79T= XP_011538135.1:n.648+79T=
XM_011539834.1:c.648+79T= XP_011538136.1:n.648+79T=
NM_001322965.1:c.648+79T= NP_001309894.1:n.648+79T=
NM_001322966.1:c.648+79T= NP_001309895.1:n.648+79T=
NM_001322967.1:c.648+79T= NP_001309896.1:n.648+79T=
NM_001322968.1:c.648+79T= NP_001309897.1:n.648+79T=
NM_001322969.1:c.648+79T= NP_001309898.1:n.648+79T=
NM_001322970.1:c.648+79T= NP_001309899.1:n.648+79T=
NM_001322971.1:c.327+79T= NP_001309900.1:n.327+79T=
NM_001322974.1:c.48+79T= NP_001309903.1:n.48+79T=
XM_017016279.1:c.48+79T= XP_016871768.1:n.48+79T=
NM_000274.4:c.648+79T= MANE Select NP_000265.1:n.648+79T=
NM_001322965.2:c.648+79T= NP_001309894.1:n.648+79T=
NM_001322966.2:c.648+79T= NP_001309895.1:n.648+79T=
NM_001322967.2:c.648+79T= NP_001309896.1:n.648+79T=
NM_001322968.2:c.648+79T= NP_001309897.1:n.648+79T=
NM_001322969.2:c.648+79T= NP_001309898.1:n.648+79T=
NM_001322970.2:c.648+79T= NP_001309899.1:n.648+79T=
NM_001322971.2:c.327+79T= NP_001309900.1:n.327+79T=
NM_001322974.2:c.48+79T= NP_001309903.1:n.48+79T=
NM_001171814.2:c.234+79T= NP_001165285.1:n.234+79T=