Canonical Allele Identifier: CA15300060

Gene: TLR10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38772244G>T , CM000666.2:g.38772244G>T	GRCh38
NC_000004.11:g.38773865G>T , CM000666.1:g.38773865G>T	GRCh37
NC_000004.10:g.38450260G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308973.9:c.*911C>A MANE Select	ENSP00000308925.4:n.*911C>A
ENST00000308973.8:c.*911C>A	ENSP00000308925.4:n.*911C>A
ENST00000361424.6:c.*911C>A	ENSP00000354459.2:n.*911C>A
ENST00000613579.4:c.*911C>A	ENSP00000478206.1:n.*911C>A
ENST00000622002.4:c.*911C>A	ENSP00000478985.1:n.*911C>A
NM_001017388.2:c.*911C>A	NP_001017388.1:n.*911C>A
NM_001195106.1:c.*911C>A	NP_001182035.1:n.*911C>A
NM_001195107.1:c.*911C>A	NP_001182036.1:n.*911C>A
NM_001195108.1:c.*911C>A	NP_001182037.1:n.*911C>A
NM_030956.3:c.*911C>A	NP_112218.2:n.*911C>A
XM_011513760.1:c.*911C>A	XP_011512062.1:n.*911C>A
XM_011513761.1:c.*911C>A	XP_011512063.1:n.*911C>A
XM_011513762.1:c.*911C>A	XP_011512064.1:n.*911C>A
XM_011513760.2:c.*911C>A	XP_011512062.1:n.*911C>A
XM_011513761.2:c.*911C>A	XP_011512063.1:n.*911C>A
XM_011513762.2:c.*911C>A	XP_011512064.1:n.*911C>A
NM_030956.4:c.*911C>A MANE Select	NP_112218.2:n.*911C>A
NM_001195108.2:c.*911C>A	NP_001182037.1:n.*911C>A
NM_001017388.3:c.*911C>A	NP_001017388.1:n.*911C>A
NM_001195106.2:c.*911C>A	NP_001182035.1:n.*911C>A
NM_001195107.2:c.*911C>A	NP_001182036.1:n.*911C>A