Canonical Allele Identifier: CA1623533204

Gene: TREM1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41276002C>A , CM000668.2:g.41276002C>A	GRCh38
NC_000006.11:g.41243740C>A , CM000668.1:g.41243740C>A	GRCh37
NC_000006.10:g.41351718C>A	NCBI36
NG_029525.1:g.15718G>T
NG_029525.2:g.15718G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244709.9:c.*123G>T MANE Select	ENSP00000244709.3:n.*123G>T
ENST00000244709.8:c.*123G>T	ENSP00000244709.3:n.*123G>T
ENST00000334475.10:c.*182G>T	ENSP00000334284.5:n.*182G>T
ENST00000589614.5:c.599+4959G>T	ENSP00000465688.1:n.599+4959G>T
ENST00000589695.1:n.503G>T
NM_001242590.1:c.*182G>T	NP_001229519.1:n.*182G>T
NM_018643.3:c.*123G>T	NP_061113.1:n.*123G>T
XM_006715117.2:c.406+6393G>T	XP_006715180.1:n.406+6393G>T
XM_011514696.1:c.599+4959G>T	XP_011512998.1:n.599+4959G>T
NM_001242590.2:c.*182G>T	NP_001229519.1:n.*182G>T
NM_018643.4:c.*123G>T	NP_061113.1:n.*123G>T
NR_136332.1:n.918G>T
XM_006715117.3:c.406+6393G>T	XP_006715180.1:n.406+6393G>T
XM_011514696.2:c.599+4959G>T	XP_011512998.1:n.599+4959G>T
XM_017010956.2:c.*123G>T	XP_016866445.1:n.*123G>T
XM_017010957.1:c.*182G>T	XP_016866446.1:n.*182G>T
NM_018643.5:c.*123G>T MANE Select	NP_061113.1:n.*123G>T
NM_001242590.3:c.*182G>T	NP_001229519.1:n.*182G>T
NR_136332.2:n.855G>T