Canonical Allele Identifier: CA1942337391

Gene: OAT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124401746C= , CM000672.2:g.124401746C=	GRCh38
NC_000010.10:g.126090315C= , CM000672.1:g.126090315C=	GRCh37
NC_000010.9:g.126080305C=	NCBI36
NG_008861.1:g.22205G= , LRG_685:g.22205G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000274.4:c.994G= MANE Select	NP_000265.1:p.Val332=
ENST00000368845.6:c.994G= MANE Select	ENSP00000357838.5:p.Val332=
NM_000274.3:c.994G= , LRG_685t1:c.994G=	NP_000265.1:p.Val332=
NM_001171814.1:c.580G=	NP_001165285.1:p.Val194=
NM_001171814.2:c.580G=	NP_001165285.1:p.Val194=
NM_001322965.1:c.994G=	NP_001309894.1:p.Val332=
NM_001322965.2:c.994G=	NP_001309894.1:p.Val332=
NM_001322966.1:c.994G=	NP_001309895.1:p.Val332=
NM_001322966.2:c.994G=	NP_001309895.1:p.Val332=
NM_001322967.1:c.994G=	NP_001309896.1:p.Val332=
NM_001322967.2:c.994G=	NP_001309896.1:p.Val332=
NM_001322968.1:c.994G=	NP_001309897.1:p.Val332=
NM_001322968.2:c.994G=	NP_001309897.1:p.Val332=
NM_001322969.1:c.994G=	NP_001309898.1:p.Val332=
NM_001322969.2:c.994G=	NP_001309898.1:p.Val332=
NM_001322970.1:c.994G=	NP_001309899.1:p.Val332=
NM_001322970.2:c.994G=	NP_001309899.1:p.Val332=
NM_001322971.1:c.673G=	NP_001309900.1:p.Val225=
NM_001322971.2:c.673G=	NP_001309900.1:p.Val225=
NM_001322974.1:c.394G=	NP_001309903.1:p.Val132=
NM_001322974.2:c.394G=	NP_001309903.1:p.Val132=
ENST00000368845.5:c.994G=	ENSP00000357838.5:p.Val332=
ENST00000467675.5:n.795G=
ENST00000471127.1:n.504G=
ENST00000539214.5:c.580G=	ENSP00000439042.1:p.Val194=
XM_006717871.2:c.994G=	XP_006717934.1:p.Val332=
XM_011539833.1:c.994G=	XP_011538135.1:p.Val332=
XM_011539834.1:c.994G=	XP_011538136.1:p.Val332=
XM_017016279.1:c.394G=	XP_016871768.1:p.Val132=