Canonical Allele Identifier: CA1942335643

Gene: OAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124397976A= , CM000672.2:g.124397976A=	GRCh38
NC_000010.10:g.126086545A= , CM000672.1:g.126086545A=	GRCh37
NC_000010.9:g.126076535A=	NCBI36
NG_008861.1:g.25975T= , LRG_685:g.25975T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368845.6:c.1286T= MANE Select	ENSP00000357838.5:p.Ile429=
ENST00000368845.5:c.1286T=	ENSP00000357838.5:p.Ile429=
ENST00000539214.5:c.872T=	ENSP00000439042.1:p.Ile291=
NM_000274.3:c.1286T= , LRG_685t1:c.1286T=	NP_000265.1:p.Ile429=
NM_001171814.1:c.872T=	NP_001165285.1:p.Ile291=
XM_006717871.2:c.1286T=	XP_006717934.1:p.Ile429=
XM_011539833.1:c.1286T=	XP_011538135.1:p.Ile429=
XM_011539834.1:c.1286T=	XP_011538136.1:p.Ile429=
NM_001322965.1:c.1286T=	NP_001309894.1:p.Ile429=
NM_001322966.1:c.1286T=	NP_001309895.1:p.Ile429=
NM_001322967.1:c.1286T=	NP_001309896.1:p.Ile429=
NM_001322968.1:c.1286T=	NP_001309897.1:p.Ile429=
NM_001322969.1:c.1286T=	NP_001309898.1:p.Ile429=
NM_001322970.1:c.1286T=	NP_001309899.1:p.Ile429=
NM_001322971.1:c.965T=	NP_001309900.1:p.Ile322=
NM_001322974.1:c.686T=	NP_001309903.1:p.Ile229=
XM_017016279.1:c.686T=	XP_016871768.1:p.Ile229=
NM_000274.4:c.1286T= MANE Select	NP_000265.1:p.Ile429=
NM_001322965.2:c.1286T=	NP_001309894.1:p.Ile429=
NM_001322966.2:c.1286T=	NP_001309895.1:p.Ile429=
NM_001322967.2:c.1286T=	NP_001309896.1:p.Ile429=
NM_001322968.2:c.1286T=	NP_001309897.1:p.Ile429=
NM_001322969.2:c.1286T=	NP_001309898.1:p.Ile429=
NM_001322970.2:c.1286T=	NP_001309899.1:p.Ile429=
NM_001322971.2:c.965T=	NP_001309900.1:p.Ile322=
NM_001322974.2:c.686T=	NP_001309903.1:p.Ile229=
NM_001171814.2:c.872T=	NP_001165285.1:p.Ile291=