Canonical Allele Identifier: CA1623463623
Community Standard Title: NM_018965.4(TREM2):c.40G= (p.Glu14=)
Gene: TREM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41163043C= , CM000668.2:g.41163043C= GRCh38
NC_000006.11:g.41130781C= , CM000668.1:g.41130781C= GRCh37
NC_000006.10:g.41238759C= NCBI36
NG_011561.1:g.5142G= , LRG_631:g.5142G=

Transcript Alleles

HGVS Amino-acid Change
NM_018965.4:c.40G= MANE Select NP_061838.1:p.Glu14=
ENST00000373113.8:c.40G= MANE Select ENSP00000362205.3:p.Glu14=
NM_001271821.1:c.40G= NP_001258750.1:p.Glu14=
NM_001271821.2:c.40G= NP_001258750.1:p.Glu14=
NM_018965.3:c.40G= , LRG_631t1:c.40G= NP_061838.1:p.Glu14=
ENST00000338469.3:c.40G= ENSP00000342651.4:p.Glu14=
ENST00000373113.7:c.40G= ENSP00000362205.3:p.Glu14=
ENST00000373122.8:c.40G= ENSP00000362214.4:p.Glu14=
XM_006715116.2:c.130G= XP_006715179.1:p.Asp44=
XR_926795.1:n.222+7480C=
XR_926795.2:n.517+7480C=
XR_926796.1:n.214+7480C=
XR_926797.1:n.188+7480C=
XR_926797.2:n.232+7480C=