Canonical Allele Identifier: CA2575605992

Gene: TRIP11

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92017671del , CM000676.2:g.92017671del	GRCh38
NC_000014.8:g.92484015del , CM000676.1:g.92484015del	GRCh37
NC_000014.7:g.91553768del	NCBI36
NG_016970.1:g.27390del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.657+12del MANE Select	ENSP00000267622.4:n.657+12del
ENST00000555516.6:c.174+12del	ENSP00000451944.1:n.174+12del
NM_004239.3:c.657+12del	NP_004230.2:n.657+12del
XM_005268215.2:c.657+12del	XP_005268272.1:n.657+12del
XM_006720321.2:c.654+12del	XP_006720384.1:n.654+12del
XM_011537361.1:c.657+12del	XP_011535663.1:n.657+12del
XR_943560.1:n.1112+12del
NM_001321851.1:c.654+12del	NP_001308780.1:n.654+12del
NM_004239.4:c.657+12del MANE Select	NP_004230.2:n.657+12del
XM_017021787.2:c.-90+12del	XP_016877276.1:n.-90+12del
XM_017021788.2:c.-542+12del	XP_016877277.1:n.-542+12del
XR_001750598.2:n.1106+12del
XR_943560.2:n.1106+12del