Canonical Allele Identifier: CA1623461336

Gene: TREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41161241G= , CM000668.2:g.41161241G=	GRCh38
NC_000006.11:g.41128979G= , CM000668.1:g.41128979G=	GRCh37
NC_000006.10:g.41236957G=	NCBI36
NG_011561.1:g.6944C= , LRG_631:g.6944C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373113.8:c.391+22C= MANE Select	ENSP00000362205.3:n.391+22C=
ENST00000338469.3:c.391+22C=	ENSP00000342651.4:n.391+22C=
ENST00000373113.7:c.391+22C=	ENSP00000362205.3:n.391+22C=
ENST00000373122.8:c.391+22C=	ENSP00000362214.4:n.391+22C=
NM_001271821.1:c.391+22C=	NP_001258750.1:n.391+22C=
NM_018965.3:c.391+22C= , LRG_631t1:c.391+22C=	NP_061838.1:n.391+22C=
XM_006715116.2:c.131-1359C=	XP_006715179.1:n.131-1359C=
XR_926795.1:n.222+5678G=
XR_926796.1:n.214+5678G=
XR_926797.1:n.188+5678G=
XR_926795.2:n.517+5678G=
XR_926797.2:n.232+5678G=
NM_001271821.2:c.391+22C=	NP_001258750.1:n.391+22C=
NM_018965.4:c.391+22C= MANE Select	NP_061838.1:n.391+22C=