Canonical Allele Identifier: CA12191930
Gene: TREM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.41277434C>T , CM000668.2:g.41277434C>T GRCh38
NC_000006.11:g.41245172C>T , CM000668.1:g.41245172C>T GRCh37
NC_000006.10:g.41353150C>T NCBI36
NG_029525.1:g.14286G>A
NG_029525.2:g.14286G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000244709.9:c.600-1204G>A MANE Select ENSP00000244709.3:n.600-1204G>A
ENST00000244709.8:c.600-1204G>A ENSP00000244709.3:n.600-1204G>A
ENST00000334475.10:c.407-1204G>A ENSP00000334284.5:n.407-1204G>A
ENST00000589614.5:c.599+3527G>A ENSP00000465688.1:n.599+3527G>A
ENST00000589695.1:n.275-1204G>A
NM_001242590.1:c.407-1204G>A NP_001229519.1:n.407-1204G>A
NM_018643.3:c.600-1204G>A NP_061113.1:n.600-1204G>A
XM_006715117.2:c.406+4961G>A XP_006715180.1:n.406+4961G>A
XM_011514696.1:c.599+3527G>A XP_011512998.1:n.599+3527G>A
NM_001242590.2:c.407-1204G>A NP_001229519.1:n.407-1204G>A
NM_018643.4:c.600-1204G>A NP_061113.1:n.600-1204G>A
NR_136332.1:n.690-1204G>A
XM_006715117.3:c.406+4961G>A XP_006715180.1:n.406+4961G>A
XM_011514696.2:c.599+3527G>A XP_011512998.1:n.599+3527G>A
XM_017010956.2:c.600-1204G>A XP_016866445.1:n.600-1204G>A
XM_017010957.1:c.407-1204G>A XP_016866446.1:n.407-1204G>A
NM_018643.5:c.600-1204G>A MANE Select NP_061113.1:n.600-1204G>A
NM_001242590.3:c.407-1204G>A NP_001229519.1:n.407-1204G>A
NR_136332.2:n.627-1204G>A