Canonical Allele Identifier: CA467037262

Gene: TLR4

Linked Data

• MyVariant Identifiers: chr9:g.120475525A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713247A>C , CM000671.2:g.117713247A>C	GRCh38
NC_000009.11:g.120475525A>C , CM000671.1:g.120475525A>C	GRCh37
NC_000009.10:g.119515346A>C	NCBI36
NG_011475.1:g.14066A>C
NG_011475.2:g.13845A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8682A>C	ENSP00000496197.1:n.93+8682A>C
ENST00000697624.1:n.200+8682A>C
ENST00000697625.1:c.93+8682A>C	ENSP00000513362.1:n.93+8682A>C
ENST00000697636.1:c.93+8682A>C	ENSP00000513366.1:n.93+8682A>C
ENST00000697637.1:c.93+8682A>C	ENSP00000513367.1:n.93+8682A>C
ENST00000697664.1:c.140+4518A>C	ENSP00000513389.1:n.140+4518A>C
ENST00000697665.1:c.93+8682A>C	ENSP00000513390.1:n.93+8682A>C
ENST00000697666.1:c.140+4518A>C	ENSP00000513391.1:n.140+4518A>C
ENST00000355622.8:c.1119A>C MANE Select	ENSP00000363089.5:p.Pro373=
ENST00000394487.5:c.999A>C	ENSP00000377997.4:p.Pro333=
ENST00000472304.2:c.*853A>C	ENSP00000496429.1:n.*853A>C
ENST00000642985.1:c.260+4518A>C	ENSP00000493686.1:n.260+4518A>C
ENST00000646089.1:c.93+8682A>C	ENSP00000496197.1:n.93+8682A>C
ENST00000665764.1:c.93+8682A>C	ENSP00000499745.1:n.93+8682A>C
ENST00000355622.6:c.1119A>C	ENSP00000363089.5:p.Pro373=
ENST00000394487.4:c.999A>C	ENSP00000377997.4:p.Pro333=
ENST00000472304.1:n.1036A>C
NM_003266.3:c.999A>C	NP_003257.1:p.Pro333=
NM_138554.4:c.1119A>C	NP_612564.1:p.Pro373=
NM_138557.2:c.519A>C	NP_612567.1:p.Pro173=
NM_138554.5:c.1119A>C MANE Select	NP_612564.1:p.Pro373=
NM_003266.4:c.999A>C	NP_003257.1:p.Pro333=
NM_138557.3:c.519A>C	NP_612567.1:p.Pro173=