Canonical Allele Identifier: CA1623461452

Gene: TREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161340_41161341delinsGC , CM000668.2:g.41161340_41161341delinsGC	GRCh38
NC_000006.11:g.41129078_41129079delinsGC , CM000668.1:g.41129078_41129079delinsGC	GRCh37
NC_000006.10:g.41237056_41237057delinsGC	NCBI36
NG_011561.1:g.6844_6845delinsGC , LRG_631:g.6844_6845delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.313_314delinsGC MANE Select	ENSP00000362205.3:p.Ala105=
ENST00000338469.3:c.313_314delinsGC	ENSP00000342651.4:p.Ala105=
ENST00000373113.7:c.313_314delinsGC	ENSP00000362205.3:p.Ala105=
ENST00000373122.8:c.313_314delinsGC	ENSP00000362214.4:p.Ala105=
NM_001271821.1:c.313_314delinsGC	NP_001258750.1:p.Ala105=
NM_018965.3:c.313_314delinsGC , LRG_631t1:c.313_314delinsGC	NP_061838.1:p.Ala105=
XM_006715116.2:c.131-1459_131-1458delinsGC	XP_006715179.1:n.131-1459_131-1458delinsG...
XR_926795.1:n.222+5777_222+5778delinsGC
XR_926796.1:n.214+5777_214+5778delinsGC
XR_926797.1:n.188+5777_188+5778delinsGC
XR_926795.2:n.517+5777_517+5778delinsGC
XR_926797.2:n.232+5777_232+5778delinsGC
NM_001271821.2:c.313_314delinsGC	NP_001258750.1:p.Ala105=
NM_018965.4:c.313_314delinsGC MANE Select	NP_061838.1:p.Ala105=