Canonical Allele Identifier: CA824738046

Gene: TREM1

Linked Data

• dbSNP Id: rs1049244602
• MyVariant Identifiers: chr6:g.41253965A>C (hg19) ; chr6:g.41286227A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.41286227A>C , CM000668.2:g.41286227A>C	GRCh38
NC_000006.11:g.41253965A>C , CM000668.1:g.41253965A>C	GRCh37
NC_000006.10:g.41361943A>C	NCBI36
NG_029525.1:g.5493T>G
NG_029525.2:g.5493T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000244709.9:c.49+380T>G MANE Select	ENSP00000244709.3:n.49+380T>G
ENST00000244709.8:c.49+380T>G	ENSP00000244709.3:n.49+380T>G
ENST00000334475.10:c.49+380T>G	ENSP00000334284.5:n.49+380T>G
ENST00000586287.1:n.76+380T>G
ENST00000589614.5:c.49+380T>G	ENSP00000465688.1:n.49+380T>G
ENST00000591620.1:c.49+380T>G	ENSP00000465345.1:n.49+380T>G
NM_001242589.1:c.49+380T>G	NP_001229518.1:n.49+380T>G
NM_001242590.1:c.49+380T>G	NP_001229519.1:n.49+380T>G
NM_018643.3:c.49+380T>G	NP_061113.1:n.49+380T>G
XM_006715117.2:c.49+380T>G	XP_006715180.1:n.49+380T>G
XM_011514696.1:c.49+380T>G	XP_011512998.1:n.49+380T>G
XM_011514697.1:c.49+380T>G	XP_011512999.1:n.49+380T>G
NM_001242589.2:c.49+380T>G	NP_001229518.1:n.49+380T>G
NM_001242590.2:c.49+380T>G	NP_001229519.1:n.49+380T>G
NM_018643.4:c.49+380T>G	NP_061113.1:n.49+380T>G
NR_136332.1:n.139+380T>G
XM_006715117.3:c.49+380T>G	XP_006715180.1:n.49+380T>G
XM_011514696.2:c.49+380T>G	XP_011512998.1:n.49+380T>G
XM_017010956.2:c.49+380T>G	XP_016866445.1:n.49+380T>G
XM_017010957.1:c.49+380T>G	XP_016866446.1:n.49+380T>G
NM_018643.5:c.49+380T>G MANE Select	NP_061113.1:n.49+380T>G
NM_001242589.3:c.49+380T>G	NP_001229518.1:n.49+380T>G
NM_001242590.3:c.49+380T>G	NP_001229519.1:n.49+380T>G
NR_136332.2:n.76+380T>G