Canonical Allele Identifier: CA374656372

Gene: TLR4

Linked Data

• MyVariant Identifiers: chr9:g.120475608T>G (hg19) ; chr9:g.117713330T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713330T>G , CM000671.2:g.117713330T>G	GRCh38
NC_000009.11:g.120475608T>G , CM000671.1:g.120475608T>G	GRCh37
NC_000009.10:g.119515429T>G	NCBI36
NG_011475.1:g.14149T>G
NG_011475.2:g.13928T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+8765T>G	ENSP00000496197.1:n.93+8765T>G
ENST00000697624.1:n.200+8765T>G
ENST00000697625.1:c.93+8765T>G	ENSP00000513362.1:n.93+8765T>G
ENST00000697636.1:c.93+8765T>G	ENSP00000513366.1:n.93+8765T>G
ENST00000697637.1:c.93+8765T>G	ENSP00000513367.1:n.93+8765T>G
ENST00000697664.1:c.140+4601T>G	ENSP00000513389.1:n.140+4601T>G
ENST00000697665.1:c.93+8765T>G	ENSP00000513390.1:n.93+8765T>G
ENST00000697666.1:c.140+4601T>G	ENSP00000513391.1:n.140+4601T>G
ENST00000355622.8:c.1202T>G MANE Select	ENSP00000363089.5:p.Leu401Arg
ENST00000394487.5:c.1082T>G	ENSP00000377997.4:p.Leu361Arg
ENST00000472304.2:c.*936T>G	ENSP00000496429.1:n.*936T>G
ENST00000642985.1:c.260+4601T>G	ENSP00000493686.1:n.260+4601T>G
ENST00000646089.1:c.93+8765T>G	ENSP00000496197.1:n.93+8765T>G
ENST00000665764.1:c.93+8765T>G	ENSP00000499745.1:n.93+8765T>G
ENST00000355622.6:c.1202T>G	ENSP00000363089.5:p.Leu401Arg
ENST00000394487.4:c.1082T>G	ENSP00000377997.4:p.Leu361Arg
ENST00000472304.1:n.1119T>G
NM_003266.3:c.1082T>G	NP_003257.1:p.Leu361Arg
NM_138554.4:c.1202T>G	NP_612564.1:p.Leu401Arg
NM_138557.2:c.602T>G	NP_612567.1:p.Leu201Arg
NM_138554.5:c.1202T>G MANE Select	NP_612564.1:p.Leu401Arg
NM_003266.4:c.1082T>G	NP_003257.1:p.Leu361Arg
NM_138557.3:c.602T>G	NP_612567.1:p.Leu201Arg