Canonical Allele Identifier: CA471762772

Gene: OAT

Linked Data

• MyVariant Identifiers: chr10:g.126091504A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124402935A>G , CM000672.2:g.124402935A>G	GRCh38
NC_000010.10:g.126091504A>G , CM000672.1:g.126091504A>G	GRCh37
NC_000010.9:g.126081494A>G	NCBI36
NG_008861.1:g.21016T>C , LRG_685:g.21016T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368845.6:c.892T>C MANE Select	ENSP00000357838.5:p.Leu298=
ENST00000368845.5:c.892T>C	ENSP00000357838.5:p.Leu298=
ENST00000467675.5:n.693T>C
ENST00000471127.1:n.402T>C
ENST00000539214.5:c.478T>C	ENSP00000439042.1:p.Leu160=
NM_000274.3:c.892T>C , LRG_685t1:c.892T>C	NP_000265.1:p.Leu298=
NM_001171814.1:c.478T>C	NP_001165285.1:p.Leu160=
XM_006717871.2:c.892T>C	XP_006717934.1:p.Leu298=
XM_011539833.1:c.892T>C	XP_011538135.1:p.Leu298=
XM_011539834.1:c.892T>C	XP_011538136.1:p.Leu298=
NM_001322965.1:c.892T>C	NP_001309894.1:p.Leu298=
NM_001322966.1:c.892T>C	NP_001309895.1:p.Leu298=
NM_001322967.1:c.892T>C	NP_001309896.1:p.Leu298=
NM_001322968.1:c.892T>C	NP_001309897.1:p.Leu298=
NM_001322969.1:c.892T>C	NP_001309898.1:p.Leu298=
NM_001322970.1:c.892T>C	NP_001309899.1:p.Leu298=
NM_001322971.1:c.571T>C	NP_001309900.1:p.Leu191=
NM_001322974.1:c.292T>C	NP_001309903.1:p.Leu98=
XM_017016279.1:c.292T>C	XP_016871768.1:p.Leu98=
NM_000274.4:c.892T>C MANE Select	NP_000265.1:p.Leu298=
NM_001322965.2:c.892T>C	NP_001309894.1:p.Leu298=
NM_001322966.2:c.892T>C	NP_001309895.1:p.Leu298=
NM_001322967.2:c.892T>C	NP_001309896.1:p.Leu298=
NM_001322968.2:c.892T>C	NP_001309897.1:p.Leu298=
NM_001322969.2:c.892T>C	NP_001309898.1:p.Leu298=
NM_001322970.2:c.892T>C	NP_001309899.1:p.Leu298=
NM_001322971.2:c.571T>C	NP_001309900.1:p.Leu191=
NM_001322974.2:c.292T>C	NP_001309903.1:p.Leu98=
NM_001171814.2:c.478T>C	NP_001165285.1:p.Leu160=