Canonical Allele Identifier: CA113968
Gene: OAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124408635_124408643del , CM000672.2:g.124408635_124408643del GRCh38
NC_000010.10:g.126097204_126097212del , CM000672.1:g.126097204_126097212del GRCh37
NC_000010.9:g.126087194_126087202del NCBI36
NG_008861.1:g.15310_15318del , LRG_685:g.15310_15318del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.425-4_429del
ENST00000368845.5:c.425-4_429del
ENST00000467675.5:n.52-4_56del
ENST00000476917.5:n.490-4_494del
ENST00000539214.5:c.11-4_15del
NM_000274.3:c.425-4_429del , LRG_685t1:c.425-4_429del
NM_001171814.1:c.11-4_15del
XM_006717871.2:c.425-4_429del
XM_011539833.1:c.425-4_429del
XM_011539834.1:c.425-4_429del
NM_001322965.1:c.425-4_429del
NM_001322966.1:c.425-4_429del
NM_001322967.1:c.425-4_429del
NM_001322968.1:c.425-4_429del
NM_001322969.1:c.425-4_429del
NM_001322970.1:c.425-4_429del
NM_001322971.1:c.200-3078_200-3070del NP_001309900.1:n.200-3078_200-3070del
NM_001322974.1:c.-290-4_-286del
XM_017016279.1:c.-2029-4_-2025del
NM_000274.4:c.425-4_429del
NM_001322965.2:c.425-4_429del
NM_001322966.2:c.425-4_429del
NM_001322967.2:c.425-4_429del
NM_001322968.2:c.425-4_429del
NM_001322969.2:c.425-4_429del
NM_001322970.2:c.425-4_429del
NM_001322971.2:c.200-3078_200-3070del NP_001309900.1:n.200-3078_200-3070del
NM_001322974.2:c.-290-4_-286del
NM_001171814.2:c.11-4_15del
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