Canonical Allele Identifier: CA471949977

Gene: OAT

Linked Data

• ClinVar Variation Id: 1951721
• ClinVar RCV Id: RCV002695101
• MyVariant Identifiers: chr10:g.126097506T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124408937T>C , CM000672.2:g.124408937T>C	GRCh38
NC_000010.10:g.126097506T>C , CM000672.1:g.126097506T>C	GRCh37
NC_000010.9:g.126087496T>C	NCBI36
NG_008861.1:g.15014A>G , LRG_685:g.15014A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368845.6:c.228A>G MANE Select	ENSP00000357838.5:p.Arg76=
ENST00000368845.5:c.228A>G	ENSP00000357838.5:p.Arg76=
ENST00000476917.5:n.293A>G
ENST00000490096.5:n.464A>G
ENST00000492376.1:n.576A>G
ENST00000539214.5:c.-187A>G	ENSP00000439042.1:n.-187A>G
NM_000274.3:c.228A>G , LRG_685t1:c.228A>G	NP_000265.1:p.Arg76=
NM_001171814.1:c.-187A>G	NP_001165285.1:n.-187A>G
XM_006717871.2:c.228A>G	XP_006717934.1:p.Arg76=
XM_011539833.1:c.228A>G	XP_011538135.1:p.Arg76=
XM_011539834.1:c.228A>G	XP_011538136.1:p.Arg76=
NM_001322965.1:c.228A>G	NP_001309894.1:p.Arg76=
NM_001322966.1:c.228A>G	NP_001309895.1:p.Arg76=
NM_001322967.1:c.228A>G	NP_001309896.1:p.Arg76=
NM_001322968.1:c.228A>G	NP_001309897.1:p.Arg76=
NM_001322969.1:c.228A>G	NP_001309898.1:p.Arg76=
NM_001322970.1:c.228A>G	NP_001309899.1:p.Arg76=
NM_001322971.1:c.199+3036A>G	NP_001309900.1:n.199+3036A>G
NM_001322974.1:c.-487A>G	NP_001309903.1:n.-487A>G
XM_017016279.1:c.-2226A>G	XP_016871768.1:n.-2226A>G
NM_000274.4:c.228A>G MANE Select	NP_000265.1:p.Arg76=
NM_001322965.2:c.228A>G	NP_001309894.1:p.Arg76=
NM_001322966.2:c.228A>G	NP_001309895.1:p.Arg76=
NM_001322967.2:c.228A>G	NP_001309896.1:p.Arg76=
NM_001322968.2:c.228A>G	NP_001309897.1:p.Arg76=
NM_001322969.2:c.228A>G	NP_001309898.1:p.Arg76=
NM_001322970.2:c.228A>G	NP_001309899.1:p.Arg76=
NM_001322971.2:c.199+3036A>G	NP_001309900.1:n.199+3036A>G
NM_001322974.2:c.-487A>G	NP_001309903.1:n.-487A>G
NM_001171814.2:c.-187A>G	NP_001165285.1:n.-187A>G