Canonical Allele Identifier: CA7314165
Community Standard Title: NM_004239.4(TRIP11):c.526C>T (p.Arg176Ter)
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92021618G>A , CM000676.2:g.92021618G>A GRCh38
NC_000014.8:g.92487962G>A , CM000676.1:g.92487962G>A GRCh37
NC_000014.7:g.91557715G>A NCBI36
NG_016970.1:g.23442C>T

Transcript Alleles

HGVS Amino-acid Change
NM_004239.4:c.526C>T MANE Select NP_004230.2:p.Arg176Ter
ENST00000267622.8:c.526C>T MANE Select ENSP00000267622.4:p.Arg176Ter
NM_001321851.1:c.523C>T NP_001308780.1:p.Arg175Ter
NM_004239.3:c.526C>T NP_004230.2:p.Arg176Ter
ENST00000555516.6:c.43C>T ENSP00000451944.1:p.Arg15Ter
XM_005268215.2:c.526C>T XP_005268272.1:p.Arg176Ter
XM_006720321.2:c.523C>T XP_006720384.1:p.Arg175Ter
XM_011537361.1:c.526C>T XP_011535663.1:p.Arg176Ter
XM_017021787.2:c.-221C>T XP_016877276.1:n.-221C>T
XM_017021788.2:c.-673C>T XP_016877277.1:n.-673C>T
XR_001750598.2:n.975C>T
XR_943560.1:n.981C>T
XR_943560.2:n.975C>T