Canonical Allele Identifier: CA1623538033

Gene: TREM1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41286058G= , CM000668.2:g.41286058G=	GRCh38
NC_000006.11:g.41253796G= , CM000668.1:g.41253796G=	GRCh37
NC_000006.10:g.41361774G=	NCBI36
NG_029525.1:g.5662C=
NG_029525.2:g.5662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244709.9:c.49+549C= MANE Select	ENSP00000244709.3:n.49+549C=
ENST00000244709.8:c.49+549C=	ENSP00000244709.3:n.49+549C=
ENST00000334475.10:c.49+549C=	ENSP00000334284.5:n.49+549C=
ENST00000586287.1:n.76+549C=
ENST00000589614.5:c.49+549C=	ENSP00000465688.1:n.49+549C=
ENST00000591620.1:c.49+549C=	ENSP00000465345.1:n.49+549C=
NM_001242589.1:c.49+549C=	NP_001229518.1:n.49+549C=
NM_001242590.1:c.49+549C=	NP_001229519.1:n.49+549C=
NM_018643.3:c.49+549C=	NP_061113.1:n.49+549C=
XM_006715117.2:c.49+549C=	XP_006715180.1:n.49+549C=
XM_011514696.1:c.49+549C=	XP_011512998.1:n.49+549C=
XM_011514697.1:c.49+549C=	XP_011512999.1:n.49+549C=
NM_001242589.2:c.49+549C=	NP_001229518.1:n.49+549C=
NM_001242590.2:c.49+549C=	NP_001229519.1:n.49+549C=
NM_018643.4:c.49+549C=	NP_061113.1:n.49+549C=
NR_136332.1:n.139+549C=
XM_006715117.3:c.49+549C=	XP_006715180.1:n.49+549C=
XM_011514696.2:c.49+549C=	XP_011512998.1:n.49+549C=
XM_017010956.2:c.49+549C=	XP_016866445.1:n.49+549C=
XM_017010957.1:c.49+549C=	XP_016866446.1:n.49+549C=
NM_018643.5:c.49+549C= MANE Select	NP_061113.1:n.49+549C=
NM_001242589.3:c.49+549C=	NP_001229518.1:n.49+549C=
NM_001242590.3:c.49+549C=	NP_001229519.1:n.49+549C=
NR_136332.2:n.76+549C=