Canonical Allele Identifier: CA439132381
Gene: TLR10 HGNC NCBI

Linked Data

dbSNP Id: rs1412177269
gnomAD v4: 4-38774637-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38774637T>C , CM000666.2:g.38774637T>C GRCh38
NC_000004.11:g.38776258T>C , CM000666.1:g.38776258T>C GRCh37
NC_000004.10:g.38452653T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000308973.9:c.954A>G MANE Select ENSP00000308925.4:p.Lys318=
ENST00000308973.8:c.954A>G ENSP00000308925.4:p.Lys318=
ENST00000361424.6:c.954A>G ENSP00000354459.2:p.Lys318=
ENST00000506111.1:c.954A>G ENSP00000421483.1:p.Lys318=
ENST00000508334.1:c.954A>G ENSP00000424923.1:p.Lys318=
ENST00000613579.4:c.954A>G ENSP00000478206.1:p.Lys318=
ENST00000622002.4:c.954A>G ENSP00000478985.1:p.Lys318=
NM_001017388.2:c.954A>G NP_001017388.1:p.Lys318=
NM_001195106.1:c.954A>G NP_001182035.1:p.Lys318=
NM_001195107.1:c.954A>G NP_001182036.1:p.Lys318=
NM_001195108.1:c.912A>G NP_001182037.1:p.Lys304=
NM_030956.3:c.954A>G NP_112218.2:p.Lys318=
XM_011513760.1:c.912A>G XP_011512062.1:p.Lys304=
XM_011513761.1:c.954A>G XP_011512063.1:p.Lys318=
XM_011513762.1:c.954A>G XP_011512064.1:p.Lys318=
XM_011513760.2:c.912A>G XP_011512062.1:p.Lys304=
XM_011513761.2:c.954A>G XP_011512063.1:p.Lys318=
XM_011513762.2:c.954A>G XP_011512064.1:p.Lys318=
NM_030956.4:c.954A>G MANE Select NP_112218.2:p.Lys318=
NM_001195108.2:c.912A>G NP_001182037.1:p.Lys304=
NM_001017388.3:c.954A>G NP_001017388.1:p.Lys318=
NM_001195106.2:c.954A>G NP_001182035.1:p.Lys318=
NM_001195107.2:c.954A>G NP_001182036.1:p.Lys318=