Canonical Allele Identifier: CA356604878

Gene: TLR10

Linked Data

• MyVariant Identifiers: chr4:g.38776105G>C (hg19) ; chr4:g.38774484G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308973.9:c.1107C>G MANE Select	ENSP00000308925.4:p.Ile369Met
ENST00000308973.8:c.1107C>G	ENSP00000308925.4:p.Ile369Met
ENST00000361424.6:c.1107C>G	ENSP00000354459.2:p.Ile369Met
ENST00000506111.1:c.1107C>G	ENSP00000421483.1:p.Ile369Met
ENST00000508334.1:c.1107C>G	ENSP00000424923.1:p.Ile369Met
ENST00000613579.4:c.1107C>G	ENSP00000478206.1:p.Ile369Met
ENST00000622002.4:c.1107C>G	ENSP00000478985.1:p.Ile369Met
NM_001017388.2:c.1107C>G	NP_001017388.1:p.Ile369Met
NM_001195106.1:c.1107C>G	NP_001182035.1:p.Ile369Met
NM_001195107.1:c.1107C>G	NP_001182036.1:p.Ile369Met
NM_001195108.1:c.1065C>G	NP_001182037.1:p.Ile355Met
NM_030956.3:c.1107C>G	NP_112218.2:p.Ile369Met
XM_011513760.1:c.1065C>G	XP_011512062.1:p.Ile355Met
XM_011513761.1:c.1107C>G	XP_011512063.1:p.Ile369Met
XM_011513762.1:c.1107C>G	XP_011512064.1:p.Ile369Met
XM_011513760.2:c.1065C>G	XP_011512062.1:p.Ile355Met
XM_011513761.2:c.1107C>G	XP_011512063.1:p.Ile369Met
XM_011513762.2:c.1107C>G	XP_011512064.1:p.Ile369Met
NM_030956.4:c.1107C>G MANE Select	NP_112218.2:p.Ile369Met
NM_001195108.2:c.1065C>G	NP_001182037.1:p.Ile355Met
NM_001017388.3:c.1107C>G	NP_001017388.1:p.Ile369Met
NM_001195106.2:c.1107C>G	NP_001182035.1:p.Ile369Met
NM_001195107.2:c.1107C>G	NP_001182036.1:p.Ile369Met