Canonical Allele Identifier: CA2155207379

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91993647_91993648delinsAT , CM000676.2:g.91993647_91993648delinsAT	GRCh38
NC_000014.8:g.92459991_92459992delinsAT , CM000676.1:g.92459991_92459992delinsAT	GRCh37
NC_000014.7:g.91529744_91529745delinsAT	NCBI36
NG_016970.1:g.51412_51413delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5160+161_5160+162delinsAT MANE Select	ENSP00000267622.4:n.5160+161_5160+162delinsAT
ENST00000554357.5:c.4306+161_4306+162delinsAT
ENST00000557017.1:c.408+161_408+162delinsAT	ENSP00000451607.1:n.408+161_408+162delinsAT
NM_004239.3:c.5160+161_5160+162delinsAT	NP_004230.2:n.5160+161_5160+162delinsAT
XM_005268214.2:c.3834+161_3834+162delinsAT	XP_005268271.1:n.3834+161_3834+162delinsAT
XM_005268215.2:c.2130+161_2130+162delinsAT	XP_005268272.1:n.2130+161_2130+162delinsAT
XM_006720321.2:c.5157+161_5157+162delinsAT	XP_006720384.1:n.5157+161_5157+162delinsAT
XR_943560.1:n.5615+161_5615+162delinsAT
NM_001321851.1:c.5157+161_5157+162delinsAT	NP_001308780.1:n.5157+161_5157+162delinsAT
NM_004239.4:c.5160+161_5160+162delinsAT MANE Select	NP_004230.2:n.5160+161_5160+162delinsAT
XM_017021787.2:c.4455+161_4455+162delinsAT	XP_016877276.1:n.4455+161_4455+162delinsAT
XM_017021788.2:c.3834+161_3834+162delinsAT	XP_016877277.1:n.3834+161_3834+162delinsAT
XR_001750598.2:n.5445+161_5445+162delinsAT
XR_943560.2:n.5609+161_5609+162delinsAT