Canonical Allele Identifier: CA1623461535

Gene: TREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161396_41161397delinsGT , CM000668.2:g.41161396_41161397delinsGT	GRCh38
NC_000006.11:g.41129134_41129135delinsGT , CM000668.1:g.41129134_41129135delinsGT	GRCh37
NC_000006.10:g.41237112_41237113delinsGT	NCBI36
NG_011561.1:g.6788_6789delinsAC , LRG_631:g.6788_6789delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.257_258delinsAC MANE Select	ENSP00000362205.3:p.Asp86=
ENST00000338469.3:c.257_258delinsAC	ENSP00000342651.4:p.Asp86=
ENST00000373113.7:c.257_258delinsAC	ENSP00000362205.3:p.Asp86=
ENST00000373122.8:c.257_258delinsAC	ENSP00000362214.4:p.Asp86=
NM_001271821.1:c.257_258delinsAC	NP_001258750.1:p.Asp86=
NM_018965.3:c.257_258delinsAC , LRG_631t1:c.257_258delinsAC	NP_061838.1:p.Asp86=
XM_006715116.2:c.131-1515_131-1514delinsAC	XP_006715179.1:n.131-1515_131-1514delinsA...
XR_926795.1:n.222+5833_222+5834delinsGT
XR_926796.1:n.214+5833_214+5834delinsGT
XR_926797.1:n.188+5833_188+5834delinsGT
XR_926795.2:n.517+5833_517+5834delinsGT
XR_926797.2:n.232+5833_232+5834delinsGT
NM_001271821.2:c.257_258delinsAC	NP_001258750.1:p.Asp86=
NM_018965.4:c.257_258delinsAC MANE Select	NP_061838.1:p.Asp86=