Canonical Allele Identifier: CA7313375
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91999405C>T , CM000676.2:g.91999405C>T GRCh38
NC_000014.8:g.92465749C>T , CM000676.1:g.92465749C>T GRCh37
NC_000014.7:g.91535502C>T NCBI36
NG_016970.1:g.45655G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000267622.8:c.4727G>A MANE Select ENSP00000267622.4:p.Arg1576His
ENST00000554357.5:c.3873G>A
NM_004239.3:c.4727G>A NP_004230.2:p.Arg1576His
XM_005268214.2:c.3401G>A XP_005268271.1:p.Arg1134His
XM_005268215.2:c.1697G>A XP_005268272.1:p.Arg566His
XM_006720321.2:c.4724G>A XP_006720384.1:p.Arg1575His
XM_011537361.1:c.4727G>A XP_011535663.1:p.Arg1576His
XR_943560.1:n.5182G>A
NM_001321851.1:c.4724G>A NP_001308780.1:p.Arg1575His
NM_004239.4:c.4727G>A MANE Select NP_004230.2:p.Arg1576His
XM_017021787.2:c.4022G>A XP_016877276.1:p.Arg1341His
XM_017021788.2:c.3401G>A XP_016877277.1:p.Arg1134His
XR_001750598.2:n.5176G>A
XR_943560.2:n.5176G>A