Canonical Allele Identifier: CA2611307198

Gene: OAT

Linked Data

• gnomAD v4: 10-124397921-ACTGAAAACAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.124397925_124397934del , CM000672.2:g.124397925_124397934del	GRCh38
NC_000010.10:g.126086494_126086503del , CM000672.1:g.126086494_126086503del	GRCh37
NC_000010.9:g.126076484_126076493del	NCBI36
NG_008861.1:g.26020_26029del , LRG_685:g.26020_26029del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368845.6:c.*11_*20del MANE Select	ENSP00000357838.5:n.*11_*20del
ENST00000368845.5:c.*11_*20del	ENSP00000357838.5:n.*11_*20del
ENST00000539214.5:c.*11_*20del	ENSP00000439042.1:n.*11_*20del
NM_000274.3:c.*11_*20del , LRG_685t1:c.*11_*20del	NP_000265.1:n.*11_*20del
NM_001171814.1:c.*11_*20del	NP_001165285.1:n.*11_*20del
XM_006717871.2:c.*11_*20del	XP_006717934.1:n.*11_*20del
XM_011539833.1:c.*11_*20del	XP_011538135.1:n.*11_*20del
XM_011539834.1:c.*11_*20del	XP_011538136.1:n.*11_*20del
NM_001322965.1:c.*11_*20del	NP_001309894.1:n.*11_*20del
NM_001322966.1:c.*11_*20del	NP_001309895.1:n.*11_*20del
NM_001322967.1:c.*11_*20del	NP_001309896.1:n.*11_*20del
NM_001322968.1:c.*11_*20del	NP_001309897.1:n.*11_*20del
NM_001322969.1:c.*11_*20del	NP_001309898.1:n.*11_*20del
NM_001322970.1:c.*11_*20del	NP_001309899.1:n.*11_*20del
NM_001322971.1:c.*11_*20del	NP_001309900.1:n.*11_*20del
NM_001322974.1:c.*11_*20del	NP_001309903.1:n.*11_*20del
XM_017016279.1:c.*11_*20del	XP_016871768.1:n.*11_*20del
NM_000274.4:c.*11_*20del MANE Select	NP_000265.1:n.*11_*20del
NM_001322965.2:c.*11_*20del	NP_001309894.1:n.*11_*20del
NM_001322966.2:c.*11_*20del	NP_001309895.1:n.*11_*20del
NM_001322967.2:c.*11_*20del	NP_001309896.1:n.*11_*20del
NM_001322968.2:c.*11_*20del	NP_001309897.1:n.*11_*20del
NM_001322969.2:c.*11_*20del	NP_001309898.1:n.*11_*20del
NM_001322970.2:c.*11_*20del	NP_001309899.1:n.*11_*20del
NM_001322971.2:c.*11_*20del	NP_001309900.1:n.*11_*20del
NM_001322974.2:c.*11_*20del	NP_001309903.1:n.*11_*20del
NM_001171814.2:c.*11_*20del	NP_001165285.1:n.*11_*20del