Canonical Allele Identifier: CA378635070

Gene: OAT

Linked Data

• MyVariant Identifiers: chr10:g.126091501A>T (hg19) ; chr10:g.124402932A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124402932A>T , CM000672.2:g.124402932A>T	GRCh38
NC_000010.10:g.126091501A>T , CM000672.1:g.126091501A>T	GRCh37
NC_000010.9:g.126081491A>T	NCBI36
NG_008861.1:g.21019T>A , LRG_685:g.21019T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368845.6:c.895T>A MANE Select	ENSP00000357838.5:p.Tyr299Asn
ENST00000368845.5:c.895T>A	ENSP00000357838.5:p.Tyr299Asn
ENST00000467675.5:n.696T>A
ENST00000471127.1:n.405T>A
ENST00000539214.5:c.481T>A	ENSP00000439042.1:p.Tyr161Asn
NM_000274.3:c.895T>A , LRG_685t1:c.895T>A	NP_000265.1:p.Tyr299Asn
NM_001171814.1:c.481T>A	NP_001165285.1:p.Tyr161Asn
XM_006717871.2:c.895T>A	XP_006717934.1:p.Tyr299Asn
XM_011539833.1:c.895T>A	XP_011538135.1:p.Tyr299Asn
XM_011539834.1:c.895T>A	XP_011538136.1:p.Tyr299Asn
NM_001322965.1:c.895T>A	NP_001309894.1:p.Tyr299Asn
NM_001322966.1:c.895T>A	NP_001309895.1:p.Tyr299Asn
NM_001322967.1:c.895T>A	NP_001309896.1:p.Tyr299Asn
NM_001322968.1:c.895T>A	NP_001309897.1:p.Tyr299Asn
NM_001322969.1:c.895T>A	NP_001309898.1:p.Tyr299Asn
NM_001322970.1:c.895T>A	NP_001309899.1:p.Tyr299Asn
NM_001322971.1:c.574T>A	NP_001309900.1:p.Tyr192Asn
NM_001322974.1:c.295T>A	NP_001309903.1:p.Tyr99Asn
XM_017016279.1:c.295T>A	XP_016871768.1:p.Tyr99Asn
NM_000274.4:c.895T>A MANE Select	NP_000265.1:p.Tyr299Asn
NM_001322965.2:c.895T>A	NP_001309894.1:p.Tyr299Asn
NM_001322966.2:c.895T>A	NP_001309895.1:p.Tyr299Asn
NM_001322967.2:c.895T>A	NP_001309896.1:p.Tyr299Asn
NM_001322968.2:c.895T>A	NP_001309897.1:p.Tyr299Asn
NM_001322969.2:c.895T>A	NP_001309898.1:p.Tyr299Asn
NM_001322970.2:c.895T>A	NP_001309899.1:p.Tyr299Asn
NM_001322971.2:c.574T>A	NP_001309900.1:p.Tyr192Asn
NM_001322974.2:c.295T>A	NP_001309903.1:p.Tyr99Asn
NM_001171814.2:c.481T>A	NP_001165285.1:p.Tyr161Asn