Canonical Allele Identifier: CA374655980
Gene: TLR4 HGNC NCBI

Linked Data

dbSNP Id: rs1202183903

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117713149A>G , CM000671.2:g.117713149A>G GRCh38
NC_000009.11:g.120475427A>G , CM000671.1:g.120475427A>G GRCh37
NC_000009.10:g.119515248A>G NCBI36
NG_011475.1:g.13968A>G
NG_011475.2:g.13747A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+8584A>G ENSP00000496197.1:n.93+8584A>G
ENST00000697624.1:n.200+8584A>G
ENST00000697625.1:c.93+8584A>G ENSP00000513362.1:n.93+8584A>G
ENST00000697636.1:c.93+8584A>G ENSP00000513366.1:n.93+8584A>G
ENST00000697637.1:c.93+8584A>G ENSP00000513367.1:n.93+8584A>G
ENST00000697664.1:c.140+4420A>G ENSP00000513389.1:n.140+4420A>G
ENST00000697665.1:c.93+8584A>G ENSP00000513390.1:n.93+8584A>G
ENST00000697666.1:c.140+4420A>G ENSP00000513391.1:n.140+4420A>G
ENST00000355622.8:c.1021A>G MANE Select ENSP00000363089.5:p.Lys341Glu
ENST00000394487.5:c.901A>G ENSP00000377997.4:p.Lys301Glu
ENST00000472304.2:c.*755A>G ENSP00000496429.1:n.*755A>G
ENST00000642985.1:c.260+4420A>G ENSP00000493686.1:n.260+4420A>G
ENST00000646089.1:c.93+8584A>G ENSP00000496197.1:n.93+8584A>G
ENST00000665764.1:c.93+8584A>G ENSP00000499745.1:n.93+8584A>G
ENST00000355622.6:c.1021A>G ENSP00000363089.5:p.Lys341Glu
ENST00000394487.4:c.901A>G ENSP00000377997.4:p.Lys301Glu
ENST00000472304.1:n.938A>G
NM_003266.3:c.901A>G NP_003257.1:p.Lys301Glu
NM_138554.4:c.1021A>G NP_612564.1:p.Lys341Glu
NM_138557.2:c.421A>G NP_612567.1:p.Lys141Glu
NM_138554.5:c.1021A>G MANE Select NP_612564.1:p.Lys341Glu
NM_003266.4:c.901A>G NP_003257.1:p.Lys301Glu
NM_138557.3:c.421A>G NP_612567.1:p.Lys141Glu