Canonical Allele Identifier: CA114002

Gene: OAT

Linked Data

• ClinVar Variation Id: 177
• ClinVar RCV Id: RCV000000200
• dbSNP Id: rs121965058
• gnomAD v2: 10-126086555-G-A
• gnomAD v4: 10-124397986-G-A
• MyVariant Identifiers: chr10:g.126086555G>A (hg19) ; chr10:g.124397986G>A (hg38)
• PubMed: PMID:1609808

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124397986G>A , CM000672.2:g.124397986G>A	GRCh38
NC_000010.10:g.126086555G>A , CM000672.1:g.126086555G>A	GRCh37
NC_000010.9:g.126076545G>A	NCBI36
NG_008861.1:g.25965C>T , LRG_685:g.25965C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368845.6:c.1276C>T MANE Select	ENSP00000357838.5:p.Arg426Ter
ENST00000368845.5:c.1276C>T	ENSP00000357838.5:p.Arg426Ter
ENST00000539214.5:c.862C>T	ENSP00000439042.1:p.Arg288Ter
NM_000274.3:c.1276C>T , LRG_685t1:c.1276C>T	NP_000265.1:p.Arg426Ter
NM_001171814.1:c.862C>T	NP_001165285.1:p.Arg288Ter
XM_006717871.2:c.1276C>T	XP_006717934.1:p.Arg426Ter
XM_011539833.1:c.1276C>T	XP_011538135.1:p.Arg426Ter
XM_011539834.1:c.1276C>T	XP_011538136.1:p.Arg426Ter
NM_001322965.1:c.1276C>T	NP_001309894.1:p.Arg426Ter
NM_001322966.1:c.1276C>T	NP_001309895.1:p.Arg426Ter
NM_001322967.1:c.1276C>T	NP_001309896.1:p.Arg426Ter
NM_001322968.1:c.1276C>T	NP_001309897.1:p.Arg426Ter
NM_001322969.1:c.1276C>T	NP_001309898.1:p.Arg426Ter
NM_001322970.1:c.1276C>T	NP_001309899.1:p.Arg426Ter
NM_001322971.1:c.955C>T	NP_001309900.1:p.Arg319Ter
NM_001322974.1:c.676C>T	NP_001309903.1:p.Arg226Ter
XM_017016279.1:c.676C>T	XP_016871768.1:p.Arg226Ter
NM_000274.4:c.1276C>T MANE Select	NP_000265.1:p.Arg426Ter
NM_001322965.2:c.1276C>T	NP_001309894.1:p.Arg426Ter
NM_001322966.2:c.1276C>T	NP_001309895.1:p.Arg426Ter
NM_001322967.2:c.1276C>T	NP_001309896.1:p.Arg426Ter
NM_001322968.2:c.1276C>T	NP_001309897.1:p.Arg426Ter
NM_001322969.2:c.1276C>T	NP_001309898.1:p.Arg426Ter
NM_001322970.2:c.1276C>T	NP_001309899.1:p.Arg426Ter
NM_001322971.2:c.955C>T	NP_001309900.1:p.Arg319Ter
NM_001322974.2:c.676C>T	NP_001309903.1:p.Arg226Ter
NM_001171814.2:c.862C>T	NP_001165285.1:p.Arg288Ter