Canonical Allele Identifier: CA378637529
Gene: OAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124408936T>A , CM000672.2:g.124408936T>A GRCh38
NC_000010.10:g.126097505T>A , CM000672.1:g.126097505T>A GRCh37
NC_000010.9:g.126087495T>A NCBI36
NG_008861.1:g.15015A>T , LRG_685:g.15015A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.229A>T MANE Select ENSP00000357838.5:p.Lys77Ter
ENST00000368845.5:c.229A>T ENSP00000357838.5:p.Lys77Ter
ENST00000476917.5:n.294A>T
ENST00000490096.5:n.465A>T
ENST00000492376.1:n.577A>T
ENST00000539214.5:c.-186A>T ENSP00000439042.1:n.-186A>T
NM_000274.3:c.229A>T , LRG_685t1:c.229A>T NP_000265.1:p.Lys77Ter
NM_001171814.1:c.-186A>T NP_001165285.1:n.-186A>T
XM_006717871.2:c.229A>T XP_006717934.1:p.Lys77Ter
XM_011539833.1:c.229A>T XP_011538135.1:p.Lys77Ter
XM_011539834.1:c.229A>T XP_011538136.1:p.Lys77Ter
NM_001322965.1:c.229A>T NP_001309894.1:p.Lys77Ter
NM_001322966.1:c.229A>T NP_001309895.1:p.Lys77Ter
NM_001322967.1:c.229A>T NP_001309896.1:p.Lys77Ter
NM_001322968.1:c.229A>T NP_001309897.1:p.Lys77Ter
NM_001322969.1:c.229A>T NP_001309898.1:p.Lys77Ter
NM_001322970.1:c.229A>T NP_001309899.1:p.Lys77Ter
NM_001322971.1:c.199+3037A>T NP_001309900.1:n.199+3037A>T
NM_001322974.1:c.-486A>T NP_001309903.1:n.-486A>T
XM_017016279.1:c.-2225A>T XP_016871768.1:n.-2225A>T
NM_000274.4:c.229A>T MANE Select NP_000265.1:p.Lys77Ter
NM_001322965.2:c.229A>T NP_001309894.1:p.Lys77Ter
NM_001322966.2:c.229A>T NP_001309895.1:p.Lys77Ter
NM_001322967.2:c.229A>T NP_001309896.1:p.Lys77Ter
NM_001322968.2:c.229A>T NP_001309897.1:p.Lys77Ter
NM_001322969.2:c.229A>T NP_001309898.1:p.Lys77Ter
NM_001322970.2:c.229A>T NP_001309899.1:p.Lys77Ter
NM_001322971.2:c.199+3037A>T NP_001309900.1:n.199+3037A>T
NM_001322974.2:c.-486A>T NP_001309903.1:n.-486A>T
NM_001171814.2:c.-186A>T NP_001165285.1:n.-186A>T