Canonical Allele Identifier: CA7314207
Gene: TRIP11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92021812T>G , CM000676.2:g.92021812T>G GRCh38
NC_000014.8:g.92488156T>G , CM000676.1:g.92488156T>G GRCh37
NC_000014.7:g.91557909T>G NCBI36
NG_016970.1:g.23248A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000267622.8:c.332A>C MANE Select ENSP00000267622.4:p.Lys111Thr
ENST00000555516.6:c.-152A>C ENSP00000451944.1:n.-152A>C
NM_004239.3:c.332A>C NP_004230.2:p.Lys111Thr
XM_005268215.2:c.332A>C XP_005268272.1:p.Lys111Thr
XM_006720321.2:c.329A>C XP_006720384.1:p.Lys110Thr
XM_011537361.1:c.332A>C XP_011535663.1:p.Lys111Thr
XR_943560.1:n.787A>C
NM_001321851.1:c.329A>C NP_001308780.1:p.Lys110Thr
NM_004239.4:c.332A>C MANE Select NP_004230.2:p.Lys111Thr
XM_017021787.2:c.-415A>C XP_016877276.1:n.-415A>C
XM_017021788.2:c.-867A>C XP_016877277.1:n.-867A>C
XR_001750598.2:n.781A>C
XR_943560.2:n.781A>C