Canonical Allele Identifier: CA374655755

Gene: TLR4

Linked Data

• COSMIC: COSM6182508
• MyVariant Identifiers: chr9:g.120475322T>G (hg19) ; chr9:g.117713044T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713044T>G , CM000671.2:g.117713044T>G	GRCh38
NC_000009.11:g.120475322T>G , CM000671.1:g.120475322T>G	GRCh37
NC_000009.10:g.119515143T>G	NCBI36
NG_011475.1:g.13863T>G
NG_011475.2:g.13642T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8479T>G	ENSP00000496197.1:n.93+8479T>G
ENST00000697624.1:n.200+8479T>G
ENST00000697625.1:c.93+8479T>G	ENSP00000513362.1:n.93+8479T>G
ENST00000697636.1:c.93+8479T>G	ENSP00000513366.1:n.93+8479T>G
ENST00000697637.1:c.93+8479T>G	ENSP00000513367.1:n.93+8479T>G
ENST00000697664.1:c.140+4315T>G	ENSP00000513389.1:n.140+4315T>G
ENST00000697665.1:c.93+8479T>G	ENSP00000513390.1:n.93+8479T>G
ENST00000697666.1:c.140+4315T>G	ENSP00000513391.1:n.140+4315T>G
ENST00000355622.8:c.916T>G MANE Select	ENSP00000363089.5:p.Cys306Gly
ENST00000394487.5:c.796T>G	ENSP00000377997.4:p.Cys266Gly
ENST00000472304.2:c.*650T>G	ENSP00000496429.1:n.*650T>G
ENST00000642985.1:c.260+4315T>G	ENSP00000493686.1:n.260+4315T>G
ENST00000646089.1:c.93+8479T>G	ENSP00000496197.1:n.93+8479T>G
ENST00000665764.1:c.93+8479T>G	ENSP00000499745.1:n.93+8479T>G
ENST00000355622.6:c.916T>G	ENSP00000363089.5:p.Cys306Gly
ENST00000394487.4:c.796T>G	ENSP00000377997.4:p.Cys266Gly
ENST00000472304.1:n.833T>G
NM_003266.3:c.796T>G	NP_003257.1:p.Cys266Gly
NM_138554.4:c.916T>G	NP_612564.1:p.Cys306Gly
NM_138557.2:c.316T>G	NP_612567.1:p.Cys106Gly
NM_138554.5:c.916T>G MANE Select	NP_612564.1:p.Cys306Gly
NM_003266.4:c.796T>G	NP_003257.1:p.Cys266Gly
NM_138557.3:c.316T>G	NP_612567.1:p.Cys106Gly