Canonical Allele Identifier: CA590171592
Gene: TLR4 HGNC NCBI

Linked Data

dbSNP Id: rs879344711

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117710464dup , CM000671.2:g.117710464dup GRCh38
NC_000009.11:g.120472742dup , CM000671.1:g.120472742dup GRCh37
NC_000009.10:g.119512563dup NCBI36
NG_011475.1:g.11283dup
NG_011475.2:g.11062dup

Transcript Alleles

HGVS Amino-acid change
ENST00000646089.2:c.93+5899dup ENSP00000496197.1:n.93+5899dup
ENST00000697624.1:n.200+5899dup
ENST00000697625.1:c.93+5899dup ENSP00000513362.1:n.93+5899dup
ENST00000697636.1:c.93+5899dup ENSP00000513366.1:n.93+5899dup
ENST00000697637.1:c.93+5899dup ENSP00000513367.1:n.93+5899dup
ENST00000697664.1:c.140+1735dup ENSP00000513389.1:n.140+1735dup
ENST00000697665.1:c.93+5899dup ENSP00000513390.1:n.93+5899dup
ENST00000697666.1:c.140+1735dup ENSP00000513391.1:n.140+1735dup
ENST00000355622.8:c.260+1735dup MANE Select ENSP00000363089.5:n.260+1735dup
ENST00000394487.5:c.140+1735dup ENSP00000377997.4:n.140+1735dup
ENST00000472304.2:c.94-1925dup ENSP00000496429.1:n.94-1925dup
ENST00000642985.1:c.260+1735dup ENSP00000493686.1:n.260+1735dup
ENST00000646089.1:c.93+5899dup ENSP00000496197.1:n.93+5899dup
ENST00000665764.1:c.93+5899dup ENSP00000499745.1:n.93+5899dup
ENST00000355622.6:c.260+1735dup ENSP00000363089.5:n.260+1735dup
ENST00000394487.4:c.140+1735dup ENSP00000377997.4:n.140+1735dup
ENST00000472304.1:n.178-1925dup
NM_003266.3:c.140+1735dup NP_003257.1:n.140+1735dup
NM_138554.4:c.260+1735dup NP_612564.1:n.260+1735dup
NM_138557.2:c.-340-1925dup NP_612567.1:n.-340-1925dup
NM_138554.5:c.260+1735dup MANE Select NP_612564.1:n.260+1735dup
NM_003266.4:c.140+1735dup NP_003257.1:n.140+1735dup
NM_138557.3:c.-340-1925dup NP_612567.1:n.-340-1925dup