Canonical Allele Identifier: CA965976428

Gene: TRIP11

Linked Data

• gnomAD v3: 14-91993518-T-TAAAAAAAAAAA
• gnomAD v4: 14-91993518-T-TAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91993521_91993522insAAAAAAAAAAA , CM000676.2:g.91993521_91993522insAAAAAAAAAAA	GRCh38
NC_000014.8:g.92459865_92459866insAAAAAAAAAAA , CM000676.1:g.92459865_92459866insAAAAAAAAAAA	GRCh37
NC_000014.7:g.91529618_91529619insAAAAAAAAAAA	NCBI36
NG_016970.1:g.51541_51542insTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5160+290_5160+291insTTTTTTTTTTT MANE Select	ENSP00000267622.4:n.5160+290_5160+291insTTTTTTTTTTT
ENST00000554357.5:c.4306+290_4306+291insTTTTTTTTTTT
ENST00000557017.1:c.408+290_408+291insTTTTTTTTTTT	ENSP00000451607.1:n.408+290_408+291insTTTTTTTTTTT
NM_004239.3:c.5160+290_5160+291insTTTTTTTTTTT	NP_004230.2:n.5160+290_5160+291insTTTTTTTTTTT
XM_005268214.2:c.3834+290_3834+291insTTTTTTTTTTT	XP_005268271.1:n.3834+290_3834+291insTTTTTTTTTTT
XM_005268215.2:c.2130+290_2130+291insTTTTTTTTTTT	XP_005268272.1:n.2130+290_2130+291insTTTTTTTTTTT
XM_006720321.2:c.5157+290_5157+291insTTTTTTTTTTT	XP_006720384.1:n.5157+290_5157+291insTTTTTTTTTTT
XR_943560.1:n.5615+290_5615+291insTTTTTTTTTTT
NM_001321851.1:c.5157+290_5157+291insTTTTTTTTTTT	NP_001308780.1:n.5157+290_5157+291insTTTTTTTTTTT
NM_004239.4:c.5160+290_5160+291insTTTTTTTTTTT MANE Select	NP_004230.2:n.5160+290_5160+291insTTTTTTTTTTT
XM_017021787.2:c.4455+290_4455+291insTTTTTTTTTTT	XP_016877276.1:n.4455+290_4455+291insTTTTTTTTTTT
XM_017021788.2:c.3834+290_3834+291insTTTTTTTTTTT	XP_016877277.1:n.3834+290_3834+291insTTTTTTTTTTT
XR_001750598.2:n.5445+290_5445+291insTTTTTTTTTTT
XR_943560.2:n.5609+290_5609+291insTTTTTTTTTTT