Canonical Allele Identifier: CA5733484
Gene: OAT HGNC NCBI

Linked Data

dbSNP Id: rs770977459

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124405454A>C , CM000672.2:g.124405454A>C GRCh38
NC_000010.10:g.126094023A>C , CM000672.1:g.126094023A>C GRCh37
NC_000010.9:g.126084013A>C NCBI36
NG_008861.1:g.18497T>G , LRG_685:g.18497T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.630T>G MANE Select ENSP00000357838.5:p.Asn210Lys
ENST00000368845.5:c.630T>G ENSP00000357838.5:p.Asn210Lys
ENST00000467675.5:n.431T>G
ENST00000483711.1:n.476T>G
ENST00000539214.5:c.216T>G ENSP00000439042.1:p.Asn72Lys
NM_000274.3:c.630T>G , LRG_685t1:c.630T>G NP_000265.1:p.Asn210Lys
NM_001171814.1:c.216T>G NP_001165285.1:p.Asn72Lys
XM_006717871.2:c.630T>G XP_006717934.1:p.Asn210Lys
XM_011539833.1:c.630T>G XP_011538135.1:p.Asn210Lys
XM_011539834.1:c.630T>G XP_011538136.1:p.Asn210Lys
NM_001322965.1:c.630T>G NP_001309894.1:p.Asn210Lys
NM_001322966.1:c.630T>G NP_001309895.1:p.Asn210Lys
NM_001322967.1:c.630T>G NP_001309896.1:p.Asn210Lys
NM_001322968.1:c.630T>G NP_001309897.1:p.Asn210Lys
NM_001322969.1:c.630T>G NP_001309898.1:p.Asn210Lys
NM_001322970.1:c.630T>G NP_001309899.1:p.Asn210Lys
NM_001322971.1:c.309T>G NP_001309900.1:p.Asn103Lys
NM_001322974.1:c.30T>G NP_001309903.1:p.Asn10Lys
XM_017016279.1:c.30T>G XP_016871768.1:p.Asn10Lys
NM_000274.4:c.630T>G MANE Select NP_000265.1:p.Asn210Lys
NM_001322965.2:c.630T>G NP_001309894.1:p.Asn210Lys
NM_001322966.2:c.630T>G NP_001309895.1:p.Asn210Lys
NM_001322967.2:c.630T>G NP_001309896.1:p.Asn210Lys
NM_001322968.2:c.630T>G NP_001309897.1:p.Asn210Lys
NM_001322969.2:c.630T>G NP_001309898.1:p.Asn210Lys
NM_001322970.2:c.630T>G NP_001309899.1:p.Asn210Lys
NM_001322971.2:c.309T>G NP_001309900.1:p.Asn103Lys
NM_001322974.2:c.30T>G NP_001309903.1:p.Asn10Lys
NM_001171814.2:c.216T>G NP_001165285.1:p.Asn72Lys