Canonical Allele Identifier: CA7313942

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92007792C>T , CM000676.2:g.92007792C>T	GRCh38
NC_000014.8:g.92474136C>T , CM000676.1:g.92474136C>T	GRCh37
NC_000014.7:g.91543889C>T	NCBI36
NG_016970.1:g.37268G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.1375G>A MANE Select	ENSP00000267622.4:p.Ala459Thr
ENST00000554357.5:c.521G>A
NM_004239.3:c.1375G>A	NP_004230.2:p.Ala459Thr
XM_005268214.2:c.49G>A	XP_005268271.1:p.Ala17Thr
XM_005268215.2:c.1375G>A	XP_005268272.1:p.Ala459Thr
XM_006720321.2:c.1372G>A	XP_006720384.1:p.Ala458Thr
XM_011537361.1:c.1375G>A	XP_011535663.1:p.Ala459Thr
XR_943560.1:n.1830G>A
NM_001321851.1:c.1372G>A	NP_001308780.1:p.Ala458Thr
NM_004239.4:c.1375G>A MANE Select	NP_004230.2:p.Ala459Thr
XM_017021787.2:c.670G>A	XP_016877276.1:p.Ala224Thr
XM_017021788.2:c.49G>A	XP_016877277.1:p.Ala17Thr
XR_001750598.2:n.1824G>A
XR_943560.2:n.1824G>A