Canonical Allele Identifier: CA1623534817

Gene: TREM1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41278735T= , CM000668.2:g.41278735T=	GRCh38
NC_000006.11:g.41246473T= , CM000668.1:g.41246473T=	GRCh37
NC_000006.10:g.41354451T=	NCBI36
NG_029525.1:g.12985A=
NG_029525.2:g.12985A=

Transcript Alleles

HGVS	Amino-acid Change
NM_018643.5:c.599+2226A= MANE Select	NP_061113.1:n.599+2226A=
ENST00000244709.9:c.599+2226A= MANE Select	ENSP00000244709.3:n.599+2226A=
NM_001242590.1:c.407-2505A=	NP_001229519.1:n.407-2505A=
NM_001242590.2:c.407-2505A=	NP_001229519.1:n.407-2505A=
NM_001242590.3:c.407-2505A=	NP_001229519.1:n.407-2505A=
NM_018643.3:c.599+2226A=	NP_061113.1:n.599+2226A=
NM_018643.4:c.599+2226A=	NP_061113.1:n.599+2226A=
NR_136332.1:n.689+2226A=
NR_136332.2:n.626+2226A=
ENST00000244709.8:c.599+2226A=	ENSP00000244709.3:n.599+2226A=
ENST00000334475.10:c.407-2505A=	ENSP00000334284.5:n.407-2505A=
ENST00000589614.5:c.599+2226A=	ENSP00000465688.1:n.599+2226A=
ENST00000589695.1:n.274+2226A=
XM_006715117.2:c.406+3660A=	XP_006715180.1:n.406+3660A=
XM_006715117.3:c.406+3660A=	XP_006715180.1:n.406+3660A=
XM_011514696.1:c.599+2226A=	XP_011512998.1:n.599+2226A=
XM_011514696.2:c.599+2226A=	XP_011512998.1:n.599+2226A=
XM_017010956.2:c.599+2226A=	XP_016866445.1:n.599+2226A=
XM_017010957.1:c.407-2505A=	XP_016866446.1:n.407-2505A=