Canonical Allele Identifier: CA390644857

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91976181G>A , CM000676.2:g.91976181G>A	GRCh38
NC_000014.8:g.92442525G>A , CM000676.1:g.92442525G>A	GRCh37
NC_000014.7:g.91512278G>A	NCBI36
NG_016970.1:g.68879C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.5269C>T MANE Select	NP_004230.2:p.Arg1757Ter
ENST00000267622.8:c.5269C>T MANE Select	ENSP00000267622.4:p.Arg1757Ter
NM_001321851.1:c.5266C>T	NP_001308780.1:p.Arg1756Ter
NM_004239.3:c.5269C>T	NP_004230.2:p.Arg1757Ter
ENST00000554357.5:c.4415C>T
ENST00000557017.1:c.640C>T	ENSP00000451607.1:n.640C>T
XM_005268214.2:c.3943C>T	XP_005268271.1:p.Arg1315Ter
XM_005268215.2:c.2239C>T	XP_005268272.1:p.Arg747Ter
XM_006720321.2:c.5266C>T	XP_006720384.1:p.Arg1756Ter
XM_017021787.2:c.4564C>T	XP_016877276.1:p.Arg1522Ter
XM_017021788.2:c.3943C>T	XP_016877277.1:p.Arg1315Ter
XR_943560.1:n.5847C>T
XR_943560.2:n.5841C>T