Canonical Allele Identifier: CA1451849169

Gene: TLR10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38778800A= , CM000666.2:g.38778800A=	GRCh38
NC_000004.11:g.38780421A= , CM000666.1:g.38780421A=	GRCh37
NC_000004.10:g.38456816A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000308973.9:c.-568-2374T= MANE Select	ENSP00000308925.4:n.-568-2374T=
ENST00000308973.8:c.-568-2374T=	ENSP00000308925.4:n.-568-2374T=
ENST00000361424.6:c.-62-3148T=	ENSP00000354459.2:n.-62-3148T=
ENST00000502321.5:c.-324-2374T=	ENSP00000427606.1:n.-324-2374T=
ENST00000507953.1:n.151+171T=
ENST00000613579.4:c.-379-2374T=	ENSP00000478206.1:n.-379-2374T=
ENST00000622002.4:c.-251-2837T=	ENSP00000478985.1:n.-251-2837T=
NM_001017388.2:c.-62-3148T=	NP_001017388.1:n.-62-3148T=
NM_001195106.1:c.-379-2374T=	NP_001182035.1:n.-379-2374T=
NM_001195107.1:c.-251-2837T=	NP_001182036.1:n.-251-2837T=
NM_001195108.1:c.-324-2374T=	NP_001182037.1:n.-324-2374T=
NM_030956.3:c.-568-2374T=	NP_112218.2:n.-568-2374T=
XM_011513760.1:c.-7-3245T=	XP_011512062.1:n.-7-3245T=
XM_011513761.1:c.-569+171T=	XP_011512063.1:n.-569+171T=
XM_011513762.1:c.-349-2593T=	XP_011512064.1:n.-349-2593T=
XM_011513760.2:c.-7-3245T=	XP_011512062.1:n.-7-3245T=
XM_011513761.2:c.-569+171T=	XP_011512063.1:n.-569+171T=
XM_011513762.2:c.-349-2593T=	XP_011512064.1:n.-349-2593T=
NM_030956.4:c.-568-2374T= MANE Select	NP_112218.2:n.-568-2374T=
NM_001195108.2:c.-324-2374T=	NP_001182037.1:n.-324-2374T=
NM_001017388.3:c.-62-3148T=	NP_001017388.1:n.-62-3148T=
NM_001195106.2:c.-379-2374T=	NP_001182035.1:n.-379-2374T=
NM_001195107.2:c.-251-2837T=	NP_001182036.1:n.-251-2837T=