Canonical Allele Identifier: CA2789814124
Gene: OAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124398224_124398225insAGA , CM000672.2:g.124398224_124398225insAGA GRCh38
NC_000010.10:g.126086793_126086794insAGA , CM000672.1:g.126086793_126086794insAGA GRCh37
NC_000010.9:g.126076783_126076784insAGA NCBI36
NG_008861.1:g.25726_25727insTCT , LRG_685:g.25726_25727insTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.1160-123_1160-122insTCT MANE Select ENSP00000357838.5:n.1160-123_1160-122insTCT
ENST00000368845.5:c.1160-123_1160-122insTCT ENSP00000357838.5:n.1160-123_1160-122insTCT
ENST00000471127.1:n.670-123_670-122insTCT
ENST00000539214.5:c.746-123_746-122insTCT ENSP00000439042.1:n.746-123_746-122insTCT
NM_000274.3:c.1160-123_1160-122insTCT , LRG_685t1:c.1160-123_1160-122insTCT NP_000265.1:n.1160-123_1160-122insTCT
NM_001171814.1:c.746-123_746-122insTCT NP_001165285.1:n.746-123_746-122insTCT
XM_006717871.2:c.1160-123_1160-122insTCT XP_006717934.1:n.1160-123_1160-122insTCT
XM_011539833.1:c.1160-123_1160-122insTCT XP_011538135.1:n.1160-123_1160-122insTCT
XM_011539834.1:c.1160-123_1160-122insTCT XP_011538136.1:n.1160-123_1160-122insTCT
NM_001322965.1:c.1160-123_1160-122insTCT NP_001309894.1:n.1160-123_1160-122insTCT
NM_001322966.1:c.1160-123_1160-122insTCT NP_001309895.1:n.1160-123_1160-122insTCT
NM_001322967.1:c.1160-123_1160-122insTCT NP_001309896.1:n.1160-123_1160-122insTCT
NM_001322968.1:c.1160-123_1160-122insTCT NP_001309897.1:n.1160-123_1160-122insTCT
NM_001322969.1:c.1160-123_1160-122insTCT NP_001309898.1:n.1160-123_1160-122insTCT
NM_001322970.1:c.1160-123_1160-122insTCT NP_001309899.1:n.1160-123_1160-122insTCT
NM_001322971.1:c.839-123_839-122insTCT NP_001309900.1:n.839-123_839-122insTCT
NM_001322974.1:c.560-123_560-122insTCT NP_001309903.1:n.560-123_560-122insTCT
XM_017016279.1:c.560-123_560-122insTCT XP_016871768.1:n.560-123_560-122insTCT
NM_000274.4:c.1160-123_1160-122insTCT MANE Select NP_000265.1:n.1160-123_1160-122insTCT
NM_001322965.2:c.1160-123_1160-122insTCT NP_001309894.1:n.1160-123_1160-122insTCT
NM_001322966.2:c.1160-123_1160-122insTCT NP_001309895.1:n.1160-123_1160-122insTCT
NM_001322967.2:c.1160-123_1160-122insTCT NP_001309896.1:n.1160-123_1160-122insTCT
NM_001322968.2:c.1160-123_1160-122insTCT NP_001309897.1:n.1160-123_1160-122insTCT
NM_001322969.2:c.1160-123_1160-122insTCT NP_001309898.1:n.1160-123_1160-122insTCT
NM_001322970.2:c.1160-123_1160-122insTCT NP_001309899.1:n.1160-123_1160-122insTCT
NM_001322971.2:c.839-123_839-122insTCT NP_001309900.1:n.839-123_839-122insTCT
NM_001322974.2:c.560-123_560-122insTCT NP_001309903.1:n.560-123_560-122insTCT
NM_001171814.2:c.746-123_746-122insTCT NP_001165285.1:n.746-123_746-122insTCT