Canonical Allele Identifier: CA2789814120
Gene: OAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124398215_124398216insACA , CM000672.2:g.124398215_124398216insACA GRCh38
NC_000010.10:g.126086784_126086785insACA , CM000672.1:g.126086784_126086785insACA GRCh37
NC_000010.9:g.126076774_126076775insACA NCBI36
NG_008861.1:g.25735_25736insTGT , LRG_685:g.25735_25736insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.1160-114_1160-113insTGT MANE Select ENSP00000357838.5:n.1160-114_1160-113insTGT
ENST00000368845.5:c.1160-114_1160-113insTGT ENSP00000357838.5:n.1160-114_1160-113insTGT
ENST00000471127.1:n.670-114_670-113insTGT
ENST00000539214.5:c.746-114_746-113insTGT ENSP00000439042.1:n.746-114_746-113insTGT
NM_000274.3:c.1160-114_1160-113insTGT , LRG_685t1:c.1160-114_1160-113insTGT NP_000265.1:n.1160-114_1160-113insTGT
NM_001171814.1:c.746-114_746-113insTGT NP_001165285.1:n.746-114_746-113insTGT
XM_006717871.2:c.1160-114_1160-113insTGT XP_006717934.1:n.1160-114_1160-113insTGT
XM_011539833.1:c.1160-114_1160-113insTGT XP_011538135.1:n.1160-114_1160-113insTGT
XM_011539834.1:c.1160-114_1160-113insTGT XP_011538136.1:n.1160-114_1160-113insTGT
NM_001322965.1:c.1160-114_1160-113insTGT NP_001309894.1:n.1160-114_1160-113insTGT
NM_001322966.1:c.1160-114_1160-113insTGT NP_001309895.1:n.1160-114_1160-113insTGT
NM_001322967.1:c.1160-114_1160-113insTGT NP_001309896.1:n.1160-114_1160-113insTGT
NM_001322968.1:c.1160-114_1160-113insTGT NP_001309897.1:n.1160-114_1160-113insTGT
NM_001322969.1:c.1160-114_1160-113insTGT NP_001309898.1:n.1160-114_1160-113insTGT
NM_001322970.1:c.1160-114_1160-113insTGT NP_001309899.1:n.1160-114_1160-113insTGT
NM_001322971.1:c.839-114_839-113insTGT NP_001309900.1:n.839-114_839-113insTGT
NM_001322974.1:c.560-114_560-113insTGT NP_001309903.1:n.560-114_560-113insTGT
XM_017016279.1:c.560-114_560-113insTGT XP_016871768.1:n.560-114_560-113insTGT
NM_000274.4:c.1160-114_1160-113insTGT MANE Select NP_000265.1:n.1160-114_1160-113insTGT
NM_001322965.2:c.1160-114_1160-113insTGT NP_001309894.1:n.1160-114_1160-113insTGT
NM_001322966.2:c.1160-114_1160-113insTGT NP_001309895.1:n.1160-114_1160-113insTGT
NM_001322967.2:c.1160-114_1160-113insTGT NP_001309896.1:n.1160-114_1160-113insTGT
NM_001322968.2:c.1160-114_1160-113insTGT NP_001309897.1:n.1160-114_1160-113insTGT
NM_001322969.2:c.1160-114_1160-113insTGT NP_001309898.1:n.1160-114_1160-113insTGT
NM_001322970.2:c.1160-114_1160-113insTGT NP_001309899.1:n.1160-114_1160-113insTGT
NM_001322971.2:c.839-114_839-113insTGT NP_001309900.1:n.839-114_839-113insTGT
NM_001322974.2:c.560-114_560-113insTGT NP_001309903.1:n.560-114_560-113insTGT
NM_001171814.2:c.746-114_746-113insTGT NP_001165285.1:n.746-114_746-113insTGT