Canonical Allele Identifier: CA265601163

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91995576_91995578del , CM000676.2:g.91995576_91995578del	GRCh38
NC_000014.8:g.92461920_92461922del , CM000676.1:g.92461920_92461922del	GRCh37
NC_000014.7:g.91531673_91531675del	NCBI36
NG_016970.1:g.49488_49490del

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.4893-57_4893-55del MANE Select	NP_004230.2:n.4893-57_4893-55del
ENST00000267622.8:c.4893-57_4893-55del MANE Select	ENSP00000267622.4:n.4893-57_4893-55del
NM_001321851.1:c.4890-57_4890-55del	NP_001308780.1:n.4890-57_4890-55del
NM_004239.3:c.4893-57_4893-55del	NP_004230.2:n.4893-57_4893-55del
ENST00000554357.5:c.4039-57_4039-55del
ENST00000557017.1:c.141-57_141-55del	ENSP00000451607.1:n.141-57_141-55del
XM_005268214.2:c.3567-57_3567-55del	XP_005268271.1:n.3567-57_3567-55del
XM_005268215.2:c.1863-57_1863-55del	XP_005268272.1:n.1863-57_1863-55del
XM_006720321.2:c.4890-57_4890-55del	XP_006720384.1:n.4890-57_4890-55del
XM_011537361.1:c.4893-1660_4893-1658del	XP_011535663.1:n.4893-1660_4893-1658del
XM_017021787.2:c.4188-57_4188-55del	XP_016877276.1:n.4188-57_4188-55del
XM_017021788.2:c.3567-57_3567-55del	XP_016877277.1:n.3567-57_3567-55del
XR_001750598.2:n.5342-1660_5342-1658del
XR_943560.1:n.5348-57_5348-55del
XR_943560.2:n.5342-57_5342-55del