Canonical Allele Identifier: CA1942335778

Gene: OAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124398260_124398261delinsCA , CM000672.2:g.124398260_124398261delinsCA	GRCh38
NC_000010.10:g.126086829_126086830delinsCA , CM000672.1:g.126086829_126086830delinsCA	GRCh37
NC_000010.9:g.126076819_126076820delinsCA	NCBI36
NG_008861.1:g.25690_25691delinsTG , LRG_685:g.25690_25691delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368845.6:c.1160-159_1160-158delinsTG MANE Select	ENSP00000357838.5:n.1160-159_1160-158delinsTG
ENST00000368845.5:c.1160-159_1160-158delinsTG	ENSP00000357838.5:n.1160-159_1160-158delinsTG
ENST00000471127.1:n.670-159_670-158delinsTG
ENST00000539214.5:c.746-159_746-158delinsTG	ENSP00000439042.1:n.746-159_746-158delinsTG
NM_000274.3:c.1160-159_1160-158delinsTG , LRG_685t1:c.1160-159_1160-158delinsTG	NP_000265.1:n.1160-159_1160-158delinsTG
NM_001171814.1:c.746-159_746-158delinsTG	NP_001165285.1:n.746-159_746-158delinsTG
XM_006717871.2:c.1160-159_1160-158delinsTG	XP_006717934.1:n.1160-159_1160-158delinsTG
XM_011539833.1:c.1160-159_1160-158delinsTG	XP_011538135.1:n.1160-159_1160-158delinsTG
XM_011539834.1:c.1160-159_1160-158delinsTG	XP_011538136.1:n.1160-159_1160-158delinsTG
NM_001322965.1:c.1160-159_1160-158delinsTG	NP_001309894.1:n.1160-159_1160-158delinsTG
NM_001322966.1:c.1160-159_1160-158delinsTG	NP_001309895.1:n.1160-159_1160-158delinsTG
NM_001322967.1:c.1160-159_1160-158delinsTG	NP_001309896.1:n.1160-159_1160-158delinsTG
NM_001322968.1:c.1160-159_1160-158delinsTG	NP_001309897.1:n.1160-159_1160-158delinsTG
NM_001322969.1:c.1160-159_1160-158delinsTG	NP_001309898.1:n.1160-159_1160-158delinsTG
NM_001322970.1:c.1160-159_1160-158delinsTG	NP_001309899.1:n.1160-159_1160-158delinsTG
NM_001322971.1:c.839-159_839-158delinsTG	NP_001309900.1:n.839-159_839-158delinsTG
NM_001322974.1:c.560-159_560-158delinsTG	NP_001309903.1:n.560-159_560-158delinsTG
XM_017016279.1:c.560-159_560-158delinsTG	XP_016871768.1:n.560-159_560-158delinsTG
NM_000274.4:c.1160-159_1160-158delinsTG MANE Select	NP_000265.1:n.1160-159_1160-158delinsTG
NM_001322965.2:c.1160-159_1160-158delinsTG	NP_001309894.1:n.1160-159_1160-158delinsTG
NM_001322966.2:c.1160-159_1160-158delinsTG	NP_001309895.1:n.1160-159_1160-158delinsTG
NM_001322967.2:c.1160-159_1160-158delinsTG	NP_001309896.1:n.1160-159_1160-158delinsTG
NM_001322968.2:c.1160-159_1160-158delinsTG	NP_001309897.1:n.1160-159_1160-158delinsTG
NM_001322969.2:c.1160-159_1160-158delinsTG	NP_001309898.1:n.1160-159_1160-158delinsTG
NM_001322970.2:c.1160-159_1160-158delinsTG	NP_001309899.1:n.1160-159_1160-158delinsTG
NM_001322971.2:c.839-159_839-158delinsTG	NP_001309900.1:n.839-159_839-158delinsTG
NM_001322974.2:c.560-159_560-158delinsTG	NP_001309903.1:n.560-159_560-158delinsTG
NM_001171814.2:c.746-159_746-158delinsTG	NP_001165285.1:n.746-159_746-158delinsTG