Canonical Allele Identifier: CA439132194

Gene: TLR10

Linked Data

• dbSNP Id: rs1282070541
• gnomAD v2: 4-38776138-A-G
• gnomAD v3: 4-38774517-A-G
• gnomAD v4: 4-38774517-A-G
• MyVariant Identifiers: chr4:g.38776138A>G (hg19) ; chr4:g.38774517A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38774517A>G , CM000666.2:g.38774517A>G	GRCh38
NC_000004.11:g.38776138A>G , CM000666.1:g.38776138A>G	GRCh37
NC_000004.10:g.38452533A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308973.9:c.1074T>C MANE Select	ENSP00000308925.4:p.Asn358=
ENST00000308973.8:c.1074T>C	ENSP00000308925.4:p.Asn358=
ENST00000361424.6:c.1074T>C	ENSP00000354459.2:p.Asn358=
ENST00000506111.1:c.1074T>C	ENSP00000421483.1:p.Asn358=
ENST00000508334.1:c.1074T>C	ENSP00000424923.1:p.Asn358=
ENST00000613579.4:c.1074T>C	ENSP00000478206.1:p.Asn358=
ENST00000622002.4:c.1074T>C	ENSP00000478985.1:p.Asn358=
NM_001017388.2:c.1074T>C	NP_001017388.1:p.Asn358=
NM_001195106.1:c.1074T>C	NP_001182035.1:p.Asn358=
NM_001195107.1:c.1074T>C	NP_001182036.1:p.Asn358=
NM_001195108.1:c.1032T>C	NP_001182037.1:p.Asn344=
NM_030956.3:c.1074T>C	NP_112218.2:p.Asn358=
XM_011513760.1:c.1032T>C	XP_011512062.1:p.Asn344=
XM_011513761.1:c.1074T>C	XP_011512063.1:p.Asn358=
XM_011513762.1:c.1074T>C	XP_011512064.1:p.Asn358=
XM_011513760.2:c.1032T>C	XP_011512062.1:p.Asn344=
XM_011513761.2:c.1074T>C	XP_011512063.1:p.Asn358=
XM_011513762.2:c.1074T>C	XP_011512064.1:p.Asn358=
NM_030956.4:c.1074T>C MANE Select	NP_112218.2:p.Asn358=
NM_001195108.2:c.1032T>C	NP_001182037.1:p.Asn344=
NM_001017388.3:c.1074T>C	NP_001017388.1:p.Asn358=
NM_001195106.2:c.1074T>C	NP_001182035.1:p.Asn358=
NM_001195107.2:c.1074T>C	NP_001182036.1:p.Asn358=