Canonical Allele Identifier: CA2670340211

Gene: TLR10

Linked Data

• gnomAD v4: 4-38778884-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38778884G>C , CM000666.2:g.38778884G>C	GRCh38
NC_000004.11:g.38780505G>C , CM000666.1:g.38780505G>C	GRCh37
NC_000004.10:g.38456900G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000308973.9:c.-568-2458C>G MANE Select	ENSP00000308925.4:n.-568-2458C>G
ENST00000308973.8:c.-568-2458C>G	ENSP00000308925.4:n.-568-2458C>G
ENST00000361424.6:c.-62-3232C>G	ENSP00000354459.2:n.-62-3232C>G
ENST00000502321.5:c.-324-2458C>G	ENSP00000427606.1:n.-324-2458C>G
ENST00000507953.1:n.151+87C>G
ENST00000613579.4:c.-379-2458C>G	ENSP00000478206.1:n.-379-2458C>G
ENST00000622002.4:c.-251-2921C>G	ENSP00000478985.1:n.-251-2921C>G
NM_001017388.2:c.-62-3232C>G	NP_001017388.1:n.-62-3232C>G
NM_001195106.1:c.-379-2458C>G	NP_001182035.1:n.-379-2458C>G
NM_001195107.1:c.-251-2921C>G	NP_001182036.1:n.-251-2921C>G
NM_001195108.1:c.-324-2458C>G	NP_001182037.1:n.-324-2458C>G
NM_030956.3:c.-568-2458C>G	NP_112218.2:n.-568-2458C>G
XM_011513760.1:c.-7-3329C>G	XP_011512062.1:n.-7-3329C>G
XM_011513761.1:c.-569+87C>G	XP_011512063.1:n.-569+87C>G
XM_011513762.1:c.-349-2677C>G	XP_011512064.1:n.-349-2677C>G
XM_011513760.2:c.-7-3329C>G	XP_011512062.1:n.-7-3329C>G
XM_011513761.2:c.-569+87C>G	XP_011512063.1:n.-569+87C>G
XM_011513762.2:c.-349-2677C>G	XP_011512064.1:n.-349-2677C>G
NM_030956.4:c.-568-2458C>G MANE Select	NP_112218.2:n.-568-2458C>G
NM_001195108.2:c.-324-2458C>G	NP_001182037.1:n.-324-2458C>G
NM_001017388.3:c.-62-3232C>G	NP_001017388.1:n.-62-3232C>G
NM_001195106.2:c.-379-2458C>G	NP_001182035.1:n.-379-2458C>G
NM_001195107.2:c.-251-2921C>G	NP_001182036.1:n.-251-2921C>G