Canonical Allele Identifier: CA439132108

Gene: TLR10

Linked Data

• dbSNP Id: rs2109306915
• gnomAD v4: 4-38774484-G-T
• MyVariant Identifiers: chr4:g.38776105G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38774484G>T , CM000666.2:g.38774484G>T	GRCh38
NC_000004.11:g.38776105G>T , CM000666.1:g.38776105G>T	GRCh37
NC_000004.10:g.38452500G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308973.9:c.1107C>A MANE Select	ENSP00000308925.4:p.Ile369=
ENST00000308973.8:c.1107C>A	ENSP00000308925.4:p.Ile369=
ENST00000361424.6:c.1107C>A	ENSP00000354459.2:p.Ile369=
ENST00000506111.1:c.1107C>A	ENSP00000421483.1:p.Ile369=
ENST00000508334.1:c.1107C>A	ENSP00000424923.1:p.Ile369=
ENST00000613579.4:c.1107C>A	ENSP00000478206.1:p.Ile369=
ENST00000622002.4:c.1107C>A	ENSP00000478985.1:p.Ile369=
NM_001017388.2:c.1107C>A	NP_001017388.1:p.Ile369=
NM_001195106.1:c.1107C>A	NP_001182035.1:p.Ile369=
NM_001195107.1:c.1107C>A	NP_001182036.1:p.Ile369=
NM_001195108.1:c.1065C>A	NP_001182037.1:p.Ile355=
NM_030956.3:c.1107C>A	NP_112218.2:p.Ile369=
XM_011513760.1:c.1065C>A	XP_011512062.1:p.Ile355=
XM_011513761.1:c.1107C>A	XP_011512063.1:p.Ile369=
XM_011513762.1:c.1107C>A	XP_011512064.1:p.Ile369=
XM_011513760.2:c.1065C>A	XP_011512062.1:p.Ile355=
XM_011513761.2:c.1107C>A	XP_011512063.1:p.Ile369=
XM_011513762.2:c.1107C>A	XP_011512064.1:p.Ile369=
NM_030956.4:c.1107C>A MANE Select	NP_112218.2:p.Ile369=
NM_001195108.2:c.1065C>A	NP_001182037.1:p.Ile355=
NM_001017388.3:c.1107C>A	NP_001017388.1:p.Ile369=
NM_001195106.2:c.1107C>A	NP_001182035.1:p.Ile369=
NM_001195107.2:c.1107C>A	NP_001182036.1:p.Ile369=