Canonical Allele Identifier: CA374655914

Gene: TLR4

Linked Data

• MyVariant Identifiers: chr9:g.120475398G>T (hg19) ; chr9:g.117713120G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713120G>T , CM000671.2:g.117713120G>T	GRCh38
NC_000009.11:g.120475398G>T , CM000671.1:g.120475398G>T	GRCh37
NC_000009.10:g.119515219G>T	NCBI36
NG_011475.1:g.13939G>T
NG_011475.2:g.13718G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8555G>T	ENSP00000496197.1:n.93+8555G>T
ENST00000697624.1:n.200+8555G>T
ENST00000697625.1:c.93+8555G>T	ENSP00000513362.1:n.93+8555G>T
ENST00000697636.1:c.93+8555G>T	ENSP00000513366.1:n.93+8555G>T
ENST00000697637.1:c.93+8555G>T	ENSP00000513367.1:n.93+8555G>T
ENST00000697664.1:c.140+4391G>T	ENSP00000513389.1:n.140+4391G>T
ENST00000697665.1:c.93+8555G>T	ENSP00000513390.1:n.93+8555G>T
ENST00000697666.1:c.140+4391G>T	ENSP00000513391.1:n.140+4391G>T
ENST00000355622.8:c.992G>T MANE Select	ENSP00000363089.5:p.Gly331Val
ENST00000394487.5:c.872G>T	ENSP00000377997.4:p.Gly291Val
ENST00000472304.2:c.*726G>T	ENSP00000496429.1:n.*726G>T
ENST00000642985.1:c.260+4391G>T	ENSP00000493686.1:n.260+4391G>T
ENST00000646089.1:c.93+8555G>T	ENSP00000496197.1:n.93+8555G>T
ENST00000665764.1:c.93+8555G>T	ENSP00000499745.1:n.93+8555G>T
ENST00000355622.6:c.992G>T	ENSP00000363089.5:p.Gly331Val
ENST00000394487.4:c.872G>T	ENSP00000377997.4:p.Gly291Val
ENST00000472304.1:n.909G>T
NM_003266.3:c.872G>T	NP_003257.1:p.Gly291Val
NM_138554.4:c.992G>T	NP_612564.1:p.Gly331Val
NM_138557.2:c.392G>T	NP_612567.1:p.Gly131Val
NM_138554.5:c.992G>T MANE Select	NP_612564.1:p.Gly331Val
NM_003266.4:c.872G>T	NP_003257.1:p.Gly291Val
NM_138557.3:c.392G>T	NP_612567.1:p.Gly131Val