Canonical Allele Identifier: CA2888990
Gene: TLR10 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11096956

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38774559C>A , CM000666.2:g.38774559C>A GRCh38
NC_000004.10:g.38452575C>A NCBI36
NC_000004.11:g.38776180C>A , CM000666.1:g.38776180C>A GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000308973.8:c.1032G>T ENSP00000308925.4:p.Pro344=
ENST00000361424.6:c.1032G>T ENSP00000354459.2:p.Pro344=
ENST00000506111.1:c.1032G>T ENSP00000421483.1:p.Pro344=
ENST00000508334.1:c.1032G>T ENSP00000424923.1:p.Pro344=
ENST00000613579.4:c.1032G>T ENSP00000478206.1:p.Pro344=
ENST00000622002.4:c.1032G>T ENSP00000478985.1:p.Pro344=
NM_001017388.2:c.1032G>T NP_001017388.1:p.Pro344=
NM_001195106.1:c.1032G>T NP_001182035.1:p.Pro344=
NM_001195107.1:c.1032G>T NP_001182036.1:p.Pro344=
NM_001195108.1:c.990G>T NP_001182037.1:p.Pro330=
NM_030956.3:c.1032G>T NP_112218.2:p.Pro344=
XM_011513760.1:c.990G>T XP_011512062.1:p.Pro330=
XM_011513761.1:c.1032G>T XP_011512063.1:p.Pro344=
XM_011513762.1:c.1032G>T XP_011512064.1:p.Pro344=