Canonical Allele Identifier: CA1623460607

Gene: TREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41160234A= , CM000668.2:g.41160234A=	GRCh38
NC_000006.11:g.41127972A= , CM000668.1:g.41127972A=	GRCh37
NC_000006.10:g.41235950A=	NCBI36
NG_011561.1:g.7951T= , LRG_631:g.7951T=

Transcript Alleles

HGVS	Amino-acid Change
NM_018965.4:c.392-352T= MANE Select	NP_061838.1:n.392-352T=
ENST00000373113.8:c.392-352T= MANE Select	ENSP00000362205.3:n.392-352T=
NM_001271821.1:c.392-352T=	NP_001258750.1:n.392-352T=
NM_001271821.2:c.392-352T=	NP_001258750.1:n.392-352T=
NM_018965.3:c.392-352T= , LRG_631t1:c.392-352T=	NP_061838.1:n.392-352T=
ENST00000338469.3:c.392-352T=	ENSP00000342651.4:n.392-352T=
ENST00000373113.7:c.392-352T=	ENSP00000362205.3:n.392-352T=
ENST00000373122.8:c.392-352T=	ENSP00000362214.4:n.392-352T=
XM_006715116.2:c.131-352T=	XP_006715179.1:n.131-352T=
XR_926795.1:n.222+4671A=
XR_926795.2:n.517+4671A=
XR_926796.1:n.214+4671A=
XR_926797.1:n.188+4671A=
XR_926797.2:n.232+4671A=