Canonical Allele Identifier: CA1875361762
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117710436G= , CM000671.2:g.117710436G= GRCh38
NC_000009.11:g.120472714G= , CM000671.1:g.120472714G= GRCh37
NC_000009.10:g.119512535G= NCBI36
NG_011475.1:g.11255G=
NG_011475.2:g.11034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+5871G= ENSP00000496197.1:n.93+5871G=
ENST00000697624.1:n.200+5871G=
ENST00000697625.1:c.93+5871G= ENSP00000513362.1:n.93+5871G=
ENST00000697636.1:c.93+5871G= ENSP00000513366.1:n.93+5871G=
ENST00000697637.1:c.93+5871G= ENSP00000513367.1:n.93+5871G=
ENST00000697664.1:c.140+1707G= ENSP00000513389.1:n.140+1707G=
ENST00000697665.1:c.93+5871G= ENSP00000513390.1:n.93+5871G=
ENST00000697666.1:c.140+1707G= ENSP00000513391.1:n.140+1707G=
ENST00000355622.8:c.260+1707G= MANE Select ENSP00000363089.5:n.260+1707G=
ENST00000394487.5:c.140+1707G= ENSP00000377997.4:n.140+1707G=
ENST00000472304.2:c.94-1953G= ENSP00000496429.1:n.94-1953G=
ENST00000642985.1:c.260+1707G= ENSP00000493686.1:n.260+1707G=
ENST00000646089.1:c.93+5871G= ENSP00000496197.1:n.93+5871G=
ENST00000665764.1:c.93+5871G= ENSP00000499745.1:n.93+5871G=
ENST00000355622.6:c.260+1707G= ENSP00000363089.5:n.260+1707G=
ENST00000394487.4:c.140+1707G= ENSP00000377997.4:n.140+1707G=
ENST00000472304.1:n.178-1953G=
NM_003266.3:c.140+1707G= NP_003257.1:n.140+1707G=
NM_138554.4:c.260+1707G= NP_612564.1:n.260+1707G=
NM_138557.2:c.-340-1953G= NP_612567.1:n.-340-1953G=
NM_138554.5:c.260+1707G= MANE Select NP_612564.1:n.260+1707G=
NM_003266.4:c.140+1707G= NP_003257.1:n.140+1707G=
NM_138557.3:c.-340-1953G= NP_612567.1:n.-340-1953G=