Canonical Allele Identifier: CA1942340672

Gene: OAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124408887C= , CM000672.2:g.124408887C=	GRCh38
NC_000010.10:g.126097456C= , CM000672.1:g.126097456C=	GRCh37
NC_000010.9:g.126087446C=	NCBI36
NG_008861.1:g.15064G= , LRG_685:g.15064G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000274.4:c.278G= MANE Select	NP_000265.1:p.Cys93=
ENST00000368845.6:c.278G= MANE Select	ENSP00000357838.5:p.Cys93=
NM_000274.3:c.278G= , LRG_685t1:c.278G=	NP_000265.1:p.Cys93=
NM_001171814.1:c.-137G=	NP_001165285.1:n.-137G=
NM_001171814.2:c.-137G=	NP_001165285.1:n.-137G=
NM_001322965.1:c.278G=	NP_001309894.1:p.Cys93=
NM_001322965.2:c.278G=	NP_001309894.1:p.Cys93=
NM_001322966.1:c.278G=	NP_001309895.1:p.Cys93=
NM_001322966.2:c.278G=	NP_001309895.1:p.Cys93=
NM_001322967.1:c.278G=	NP_001309896.1:p.Cys93=
NM_001322967.2:c.278G=	NP_001309896.1:p.Cys93=
NM_001322968.1:c.278G=	NP_001309897.1:p.Cys93=
NM_001322968.2:c.278G=	NP_001309897.1:p.Cys93=
NM_001322969.1:c.278G=	NP_001309898.1:p.Cys93=
NM_001322969.2:c.278G=	NP_001309898.1:p.Cys93=
NM_001322970.1:c.278G=	NP_001309899.1:p.Cys93=
NM_001322970.2:c.278G=	NP_001309899.1:p.Cys93=
NM_001322971.1:c.199+3086G=	NP_001309900.1:n.199+3086G=
NM_001322971.2:c.199+3086G=	NP_001309900.1:n.199+3086G=
NM_001322974.1:c.-437G=	NP_001309903.1:n.-437G=
NM_001322974.2:c.-437G=	NP_001309903.1:n.-437G=
ENST00000368845.5:c.278G=	ENSP00000357838.5:p.Cys93=
ENST00000476917.5:n.343G=
ENST00000490096.5:n.514G=
ENST00000539214.5:c.-137G=	ENSP00000439042.1:n.-137G=
XM_006717871.2:c.278G=	XP_006717934.1:p.Cys93=
XM_011539833.1:c.278G=	XP_011538135.1:p.Cys93=
XM_011539834.1:c.278G=	XP_011538136.1:p.Cys93=
XM_017016279.1:c.-2176G=	XP_016871768.1:n.-2176G=