Canonical Allele Identifier: CA378633626

Gene: OAT

Linked Data

• dbSNP Id: rs1589697471
• MyVariant Identifiers: chr10:g.126089469C>T (hg19) ; chr10:g.124400900C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124400900C>T , CM000672.2:g.124400900C>T	GRCh38
NC_000010.10:g.126089469C>T , CM000672.1:g.126089469C>T	GRCh37
NC_000010.9:g.126079459C>T	NCBI36
NG_008861.1:g.23051G>A , LRG_685:g.23051G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368845.6:c.1099G>A MANE Select	ENSP00000357838.5:p.Val367Ile
ENST00000368845.5:c.1099G>A	ENSP00000357838.5:p.Val367Ile
ENST00000471127.1:n.609G>A
ENST00000539214.5:c.685G>A	ENSP00000439042.1:p.Val229Ile
NM_000274.3:c.1099G>A , LRG_685t1:c.1099G>A	NP_000265.1:p.Val367Ile
NM_001171814.1:c.685G>A	NP_001165285.1:p.Val229Ile
XM_006717871.2:c.1099G>A	XP_006717934.1:p.Val367Ile
XM_011539833.1:c.1099G>A	XP_011538135.1:p.Val367Ile
XM_011539834.1:c.1099G>A	XP_011538136.1:p.Val367Ile
NM_001322965.1:c.1099G>A	NP_001309894.1:p.Val367Ile
NM_001322966.1:c.1099G>A	NP_001309895.1:p.Val367Ile
NM_001322967.1:c.1099G>A	NP_001309896.1:p.Val367Ile
NM_001322968.1:c.1099G>A	NP_001309897.1:p.Val367Ile
NM_001322969.1:c.1099G>A	NP_001309898.1:p.Val367Ile
NM_001322970.1:c.1099G>A	NP_001309899.1:p.Val367Ile
NM_001322971.1:c.778G>A	NP_001309900.1:p.Val260Ile
NM_001322974.1:c.499G>A	NP_001309903.1:p.Val167Ile
XM_017016279.1:c.499G>A	XP_016871768.1:p.Val167Ile
NM_000274.4:c.1099G>A MANE Select	NP_000265.1:p.Val367Ile
NM_001322965.2:c.1099G>A	NP_001309894.1:p.Val367Ile
NM_001322966.2:c.1099G>A	NP_001309895.1:p.Val367Ile
NM_001322967.2:c.1099G>A	NP_001309896.1:p.Val367Ile
NM_001322968.2:c.1099G>A	NP_001309897.1:p.Val367Ile
NM_001322969.2:c.1099G>A	NP_001309898.1:p.Val367Ile
NM_001322970.2:c.1099G>A	NP_001309899.1:p.Val367Ile
NM_001322971.2:c.778G>A	NP_001309900.1:p.Val260Ile
NM_001322974.2:c.499G>A	NP_001309903.1:p.Val167Ile
NM_001171814.2:c.685G>A	NP_001165285.1:p.Val229Ile