Canonical Allele Identifier: CA15595389
Gene: TLR4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117711556A>G , CM000671.2:g.117711556A>G GRCh38
NC_000009.11:g.120473834A>G , CM000671.1:g.120473834A>G GRCh37
NC_000009.10:g.119513655A>G NCBI36
NG_011475.1:g.12375A>G
NG_011475.2:g.12154A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+6991A>G ENSP00000496197.1:n.93+6991A>G
ENST00000697624.1:n.200+6991A>G
ENST00000697625.1:c.93+6991A>G ENSP00000513362.1:n.93+6991A>G
ENST00000697636.1:c.93+6991A>G ENSP00000513366.1:n.93+6991A>G
ENST00000697637.1:c.93+6991A>G ENSP00000513367.1:n.93+6991A>G
ENST00000697664.1:c.140+2827A>G ENSP00000513389.1:n.140+2827A>G
ENST00000697665.1:c.93+6991A>G ENSP00000513390.1:n.93+6991A>G
ENST00000697666.1:c.140+2827A>G ENSP00000513391.1:n.140+2827A>G
ENST00000355622.8:c.261-833A>G MANE Select ENSP00000363089.5:n.261-833A>G
ENST00000394487.5:c.141-833A>G ENSP00000377997.4:n.141-833A>G
ENST00000472304.2:c.94-833A>G ENSP00000496429.1:n.94-833A>G
ENST00000642985.1:c.260+2827A>G ENSP00000493686.1:n.260+2827A>G
ENST00000646089.1:c.93+6991A>G ENSP00000496197.1:n.93+6991A>G
ENST00000665764.1:c.93+6991A>G ENSP00000499745.1:n.93+6991A>G
ENST00000355622.6:c.261-833A>G ENSP00000363089.5:n.261-833A>G
ENST00000394487.4:c.141-833A>G ENSP00000377997.4:n.141-833A>G
ENST00000472304.1:n.178-833A>G
NM_003266.3:c.141-833A>G NP_003257.1:n.141-833A>G
NM_138554.4:c.261-833A>G NP_612564.1:n.261-833A>G
NM_138557.2:c.-340-833A>G NP_612567.1:n.-340-833A>G
NM_138554.5:c.261-833A>G MANE Select NP_612564.1:n.261-833A>G
NM_003266.4:c.141-833A>G NP_003257.1:n.141-833A>G
NM_138557.3:c.-340-833A>G NP_612567.1:n.-340-833A>G
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