Canonical Allele Identifier: CA1451835903

Gene: TLR10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38774560G= , CM000666.2:g.38774560G=	GRCh38
NC_000004.11:g.38776181G= , CM000666.1:g.38776181G=	GRCh37
NC_000004.10:g.38452576G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000308973.9:c.1031C= MANE Select	ENSP00000308925.4:p.Pro344=
ENST00000308973.8:c.1031C=	ENSP00000308925.4:p.Pro344=
ENST00000361424.6:c.1031C=	ENSP00000354459.2:p.Pro344=
ENST00000506111.1:c.1031C=	ENSP00000421483.1:p.Pro344=
ENST00000508334.1:c.1031C=	ENSP00000424923.1:p.Pro344=
ENST00000613579.4:c.1031C=	ENSP00000478206.1:p.Pro344=
ENST00000622002.4:c.1031C=	ENSP00000478985.1:p.Pro344=
NM_001017388.2:c.1031C=	NP_001017388.1:p.Pro344=
NM_001195106.1:c.1031C=	NP_001182035.1:p.Pro344=
NM_001195107.1:c.1031C=	NP_001182036.1:p.Pro344=
NM_001195108.1:c.989C=	NP_001182037.1:p.Pro330=
NM_030956.3:c.1031C=	NP_112218.2:p.Pro344=
XM_011513760.1:c.989C=	XP_011512062.1:p.Pro330=
XM_011513761.1:c.1031C=	XP_011512063.1:p.Pro344=
XM_011513762.1:c.1031C=	XP_011512064.1:p.Pro344=
XM_011513760.2:c.989C=	XP_011512062.1:p.Pro330=
XM_011513761.2:c.1031C=	XP_011512063.1:p.Pro344=
XM_011513762.2:c.1031C=	XP_011512064.1:p.Pro344=
NM_030956.4:c.1031C= MANE Select	NP_112218.2:p.Pro344=
NM_001195108.2:c.989C=	NP_001182037.1:p.Pro330=
NM_001017388.3:c.1031C=	NP_001017388.1:p.Pro344=
NM_001195106.2:c.1031C=	NP_001182035.1:p.Pro344=
NM_001195107.2:c.1031C=	NP_001182036.1:p.Pro344=