Canonical Allele Identifier: CA265611506

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92005419G>A , CM000676.2:g.92005419G>A	GRCh38
NC_000014.8:g.92471763G>A , CM000676.1:g.92471763G>A	GRCh37
NC_000014.7:g.91541516G>A	NCBI36
NG_016970.1:g.39641C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.2557C>T MANE Select	NP_004230.2:p.Arg853Ter
ENST00000267622.8:c.2557C>T MANE Select	ENSP00000267622.4:p.Arg853Ter
NM_001321851.1:c.2554C>T	NP_001308780.1:p.Arg852Ter
NM_004239.3:c.2557C>T	NP_004230.2:p.Arg853Ter
ENST00000554357.5:c.1703C>T
XM_005268214.2:c.1231C>T	XP_005268271.1:p.Arg411Ter
XM_005268215.2:c.1527+2221C>T	XP_005268272.1:n.1527+2221C>T
XM_006720321.2:c.2554C>T	XP_006720384.1:p.Arg852Ter
XM_011537361.1:c.2557C>T	XP_011535663.1:p.Arg853Ter
XM_017021787.2:c.1852C>T	XP_016877276.1:p.Arg618Ter
XM_017021788.2:c.1231C>T	XP_016877277.1:p.Arg411Ter
XR_001750598.2:n.3006C>T
XR_943560.1:n.3012C>T
XR_943560.2:n.3006C>T