Canonical Allele Identifier: CA12268664
Gene: TREM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41278895A>G , CM000668.2:g.41278895A>G GRCh38
NC_000006.11:g.41246633A>G , CM000668.1:g.41246633A>G GRCh37
NC_000006.10:g.41354611A>G NCBI36
NG_029525.1:g.12825T>C
NG_029525.2:g.12825T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000244709.9:c.599+2066T>C MANE Select ENSP00000244709.3:n.599+2066T>C
ENST00000244709.8:c.599+2066T>C ENSP00000244709.3:n.599+2066T>C
ENST00000334475.10:c.407-2665T>C ENSP00000334284.5:n.407-2665T>C
ENST00000589614.5:c.599+2066T>C ENSP00000465688.1:n.599+2066T>C
ENST00000589695.1:n.274+2066T>C
NM_001242590.1:c.407-2665T>C NP_001229519.1:n.407-2665T>C
NM_018643.3:c.599+2066T>C NP_061113.1:n.599+2066T>C
XM_006715117.2:c.406+3500T>C XP_006715180.1:n.406+3500T>C
XM_011514696.1:c.599+2066T>C XP_011512998.1:n.599+2066T>C
NM_001242590.2:c.407-2665T>C NP_001229519.1:n.407-2665T>C
NM_018643.4:c.599+2066T>C NP_061113.1:n.599+2066T>C
NR_136332.1:n.689+2066T>C
XM_006715117.3:c.406+3500T>C XP_006715180.1:n.406+3500T>C
XM_011514696.2:c.599+2066T>C XP_011512998.1:n.599+2066T>C
XM_017010956.2:c.599+2066T>C XP_016866445.1:n.599+2066T>C
XM_017010957.1:c.407-2665T>C XP_016866446.1:n.407-2665T>C
NM_018643.5:c.599+2066T>C MANE Select NP_061113.1:n.599+2066T>C
NM_001242590.3:c.407-2665T>C NP_001229519.1:n.407-2665T>C
NR_136332.2:n.626+2066T>C
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