Canonical Allele Identifier: CA2499222783

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91975091A>T , CM000676.2:g.91975091A>T	GRCh38
NC_000014.8:g.92441435A>T , CM000676.1:g.92441435A>T	GRCh37
NC_000014.7:g.91511188A>T	NCBI36
NG_016970.1:g.69969T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.5457+81T>A MANE Select	NP_004230.2:n.5457+81T>A
ENST00000267622.8:c.5457+81T>A MANE Select	ENSP00000267622.4:n.5457+81T>A
NM_001321851.1:c.5454+81T>A	NP_001308780.1:n.5454+81T>A
NM_004239.3:c.5457+81T>A	NP_004230.2:n.5457+81T>A
ENST00000554357.5:c.4603+81T>A
XM_005268214.2:c.4131+81T>A	XP_005268271.1:n.4131+81T>A
XM_005268215.2:c.2427+81T>A	XP_005268272.1:n.2427+81T>A
XM_006720321.2:c.5454+81T>A	XP_006720384.1:n.5454+81T>A
XM_017021787.2:c.4752+81T>A	XP_016877276.1:n.4752+81T>A
XM_017021788.2:c.4131+81T>A	XP_016877277.1:n.4131+81T>A
XR_943560.1:n.6035+81T>A
XR_943560.2:n.6029+81T>A