Canonical Allele Identifier: CA1942337414

Gene: OAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124401785G= , CM000672.2:g.124401785G=	GRCh38
NC_000010.10:g.126090354G= , CM000672.1:g.126090354G=	GRCh37
NC_000010.9:g.126080344G=	NCBI36
NG_008861.1:g.22166C= , LRG_685:g.22166C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000274.4:c.955C= MANE Select	NP_000265.1:p.His319=
ENST00000368845.6:c.955C= MANE Select	ENSP00000357838.5:p.His319=
NM_000274.3:c.955C= , LRG_685t1:c.955C=	NP_000265.1:p.His319=
NM_001171814.1:c.541C=	NP_001165285.1:p.His181=
NM_001171814.2:c.541C=	NP_001165285.1:p.His181=
NM_001322965.1:c.955C=	NP_001309894.1:p.His319=
NM_001322965.2:c.955C=	NP_001309894.1:p.His319=
NM_001322966.1:c.955C=	NP_001309895.1:p.His319=
NM_001322966.2:c.955C=	NP_001309895.1:p.His319=
NM_001322967.1:c.955C=	NP_001309896.1:p.His319=
NM_001322967.2:c.955C=	NP_001309896.1:p.His319=
NM_001322968.1:c.955C=	NP_001309897.1:p.His319=
NM_001322968.2:c.955C=	NP_001309897.1:p.His319=
NM_001322969.1:c.955C=	NP_001309898.1:p.His319=
NM_001322969.2:c.955C=	NP_001309898.1:p.His319=
NM_001322970.1:c.955C=	NP_001309899.1:p.His319=
NM_001322970.2:c.955C=	NP_001309899.1:p.His319=
NM_001322971.1:c.634C=	NP_001309900.1:p.His212=
NM_001322971.2:c.634C=	NP_001309900.1:p.His212=
NM_001322974.1:c.355C=	NP_001309903.1:p.His119=
NM_001322974.2:c.355C=	NP_001309903.1:p.His119=
ENST00000368845.5:c.955C=	ENSP00000357838.5:p.His319=
ENST00000467675.5:n.756C=
ENST00000471127.1:n.465C=
ENST00000539214.5:c.541C=	ENSP00000439042.1:p.His181=
XM_006717871.2:c.955C=	XP_006717934.1:p.His319=
XM_011539833.1:c.955C=	XP_011538135.1:p.His319=
XM_011539834.1:c.955C=	XP_011538136.1:p.His319=
XM_017016279.1:c.355C=	XP_016871768.1:p.His119=