Canonical Allele Identifier: CA2740737667

Gene: TREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161394_41161395insGG , CM000668.2:g.41161394_41161395insGG	GRCh38
NC_000006.11:g.41129132_41129133insGG , CM000668.1:g.41129132_41129133insGG	GRCh37
NC_000006.10:g.41237110_41237111insGG	NCBI36
NG_011561.1:g.6790_6791insCC , LRG_631:g.6790_6791insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.259_260insCC MANE Select	ENSP00000362205.3:p.Asp87AlafsTer?
ENST00000338469.3:c.259_260insCC	ENSP00000342651.4:p.Asp87AlafsTer?
ENST00000373113.7:c.259_260insCC	ENSP00000362205.3:p.Asp87AlafsTer?
ENST00000373122.8:c.259_260insCC	ENSP00000362214.4:p.Asp87AlafsTer?
NM_001271821.1:c.259_260insCC	NP_001258750.1:p.Asp87AlafsTer?
NM_018965.3:c.259_260insCC , LRG_631t1:c.259_260insCC	NP_061838.1:p.Asp87AlafsTer?
XM_006715116.2:c.131-1513_131-1512insCC	XP_006715179.1:n.131-1513_131-1512insCC
XR_926795.1:n.222+5831_222+5832insGG
XR_926796.1:n.214+5831_214+5832insGG
XR_926797.1:n.188+5831_188+5832insGG
XR_926795.2:n.517+5831_517+5832insGG
XR_926797.2:n.232+5831_232+5832insGG
NM_001271821.2:c.259_260insCC	NP_001258750.1:p.Asp87AlafsTer?
NM_018965.4:c.259_260insCC MANE Select	NP_061838.1:p.Asp87AlafsTer?