Canonical Allele Identifier: CA215242272

Gene: OAT

Linked Data

• dbSNP Id: rs889343713
• gnomAD v2: 10-126086948-GCACCTGTAGTCC-G
• gnomAD v3: 10-124398379-GCACCTGTAGTCC-G
• gnomAD v4: 10-124398379-GCACCTGTAGTCC-G
• MyVariant Identifiers: chr10:g.126086949_126086960del (hg19) ; chr10:g.124398380_124398391del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124398382_124398393del , CM000672.2:g.124398382_124398393del	GRCh38
NC_000010.10:g.126086951_126086962del , CM000672.1:g.126086951_126086962del	GRCh37
NC_000010.9:g.126076941_126076952del	NCBI36
NG_008861.1:g.25560_25571del , LRG_685:g.25560_25571del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368845.6:c.1160-289_1160-278del MANE Select	ENSP00000357838.5:n.1160-289_1160-278del
ENST00000368845.5:c.1160-289_1160-278del	ENSP00000357838.5:n.1160-289_1160-278del
ENST00000471127.1:n.670-289_670-278del
ENST00000539214.5:c.746-289_746-278del	ENSP00000439042.1:n.746-289_746-278del
NM_000274.3:c.1160-289_1160-278del , LRG_685t1:c.1160-289_1160-278del	NP_000265.1:n.1160-289_1160-278del
NM_001171814.1:c.746-289_746-278del	NP_001165285.1:n.746-289_746-278del
XM_006717871.2:c.1160-289_1160-278del	XP_006717934.1:n.1160-289_1160-278del
XM_011539833.1:c.1160-289_1160-278del	XP_011538135.1:n.1160-289_1160-278del
XM_011539834.1:c.1160-289_1160-278del	XP_011538136.1:n.1160-289_1160-278del
NM_001322965.1:c.1160-289_1160-278del	NP_001309894.1:n.1160-289_1160-278del
NM_001322966.1:c.1160-289_1160-278del	NP_001309895.1:n.1160-289_1160-278del
NM_001322967.1:c.1160-289_1160-278del	NP_001309896.1:n.1160-289_1160-278del
NM_001322968.1:c.1160-289_1160-278del	NP_001309897.1:n.1160-289_1160-278del
NM_001322969.1:c.1160-289_1160-278del	NP_001309898.1:n.1160-289_1160-278del
NM_001322970.1:c.1160-289_1160-278del	NP_001309899.1:n.1160-289_1160-278del
NM_001322971.1:c.839-289_839-278del	NP_001309900.1:n.839-289_839-278del
NM_001322974.1:c.560-289_560-278del	NP_001309903.1:n.560-289_560-278del
XM_017016279.1:c.560-289_560-278del	XP_016871768.1:n.560-289_560-278del
NM_000274.4:c.1160-289_1160-278del MANE Select	NP_000265.1:n.1160-289_1160-278del
NM_001322965.2:c.1160-289_1160-278del	NP_001309894.1:n.1160-289_1160-278del
NM_001322966.2:c.1160-289_1160-278del	NP_001309895.1:n.1160-289_1160-278del
NM_001322967.2:c.1160-289_1160-278del	NP_001309896.1:n.1160-289_1160-278del
NM_001322968.2:c.1160-289_1160-278del	NP_001309897.1:n.1160-289_1160-278del
NM_001322969.2:c.1160-289_1160-278del	NP_001309898.1:n.1160-289_1160-278del
NM_001322970.2:c.1160-289_1160-278del	NP_001309899.1:n.1160-289_1160-278del
NM_001322971.2:c.839-289_839-278del	NP_001309900.1:n.839-289_839-278del
NM_001322974.2:c.560-289_560-278del	NP_001309903.1:n.560-289_560-278del
NM_001171814.2:c.746-289_746-278del	NP_001165285.1:n.746-289_746-278del