Canonical Allele Identifier: CA7313593
Community Standard Title: NM_004239.4(TRIP11):c.3671G>A (p.Trp1224Ter)
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92004305C>T , CM000676.2:g.92004305C>T GRCh38
NC_000014.8:g.92470649C>T , CM000676.1:g.92470649C>T GRCh37
NC_000014.7:g.91540402C>T NCBI36
NG_016970.1:g.40755G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004239.4:c.3671G>A MANE Select NP_004230.2:p.Trp1224Ter
ENST00000267622.8:c.3671G>A MANE Select ENSP00000267622.4:p.Trp1224Ter
NM_001321851.1:c.3668G>A NP_001308780.1:p.Trp1223Ter
NM_004239.3:c.3671G>A NP_004230.2:p.Trp1224Ter
ENST00000554357.5:c.2817G>A
XM_005268214.2:c.2345G>A XP_005268271.1:p.Trp782Ter
XM_005268215.2:c.1527+3335G>A XP_005268272.1:n.1527+3335G>A
XM_006720321.2:c.3668G>A XP_006720384.1:p.Trp1223Ter
XM_011537361.1:c.3671G>A XP_011535663.1:p.Trp1224Ter
XM_017021787.2:c.2966G>A XP_016877276.1:p.Trp989Ter
XM_017021788.2:c.2345G>A XP_016877277.1:p.Trp782Ter
XR_001750598.2:n.4120G>A
XR_943560.1:n.4126G>A
XR_943560.2:n.4120G>A