Canonical Allele Identifier: CA2678673808

Gene: TREM2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41163038_41163040dup , CM000668.2:g.41163038_41163040dup	GRCh38
NC_000006.11:g.41130776_41130778dup , CM000668.1:g.41130776_41130778dup	GRCh37
NC_000006.10:g.41238754_41238756dup	NCBI36
NG_011561.1:g.5146_5148dup , LRG_631:g.5146_5148dup

Transcript Alleles

HGVS	Amino-acid Change
NM_018965.4:c.40+4_40+6dup MANE Select	NP_061838.1:n.40+4_40+6dup
ENST00000373113.8:c.40+4_40+6dup MANE Select	ENSP00000362205.3:n.40+4_40+6dup
NM_001271821.1:c.40+4_40+6dup	NP_001258750.1:n.40+4_40+6dup
NM_001271821.2:c.40+4_40+6dup	NP_001258750.1:n.40+4_40+6dup
NM_018965.3:c.40+4_40+6dup , LRG_631t1:c.40+4_40+6dup	NP_061838.1:n.40+4_40+6dup
ENST00000338469.3:c.40+4_40+6dup	ENSP00000342651.4:n.40+4_40+6dup
ENST00000373113.7:c.40+4_40+6dup	ENSP00000362205.3:n.40+4_40+6dup
ENST00000373122.8:c.40+4_40+6dup	ENSP00000362214.4:n.40+4_40+6dup
XM_006715116.2:c.130+4_130+6dup	XP_006715179.1:n.130+4_130+6dup
XR_926795.1:n.222+7475_222+7477dup
XR_926795.2:n.517+7475_517+7477dup
XR_926796.1:n.214+7475_214+7477dup
XR_926797.1:n.188+7475_188+7477dup
XR_926797.2:n.232+7475_232+7477dup