Canonical Allele Identifier: CA1875350054

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117710464_117710465delinsTC , CM000671.2:g.117710464_117710465delinsTC	GRCh38
NC_000009.11:g.120472742_120472743delinsTC , CM000671.1:g.120472742_120472743delinsTC	GRCh37
NC_000009.10:g.119512563_119512564delinsTC	NCBI36
NG_011475.1:g.11283_11284delinsTC
NG_011475.2:g.11062_11063delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+5899_93+5900delinsTC	ENSP00000496197.1:n.93+5899_93+5900delins...
ENST00000697624.1:n.200+5899_200+5900delinsTC
ENST00000697625.1:c.93+5899_93+5900delinsTC	ENSP00000513362.1:n.93+5899_93+5900delins...
ENST00000697636.1:c.93+5899_93+5900delinsTC	ENSP00000513366.1:n.93+5899_93+5900delins...
ENST00000697637.1:c.93+5899_93+5900delinsTC	ENSP00000513367.1:n.93+5899_93+5900delins...
ENST00000697664.1:c.140+1735_140+1736delinsTC	ENSP00000513389.1:n.140+1735_140+1736deli...
ENST00000697665.1:c.93+5899_93+5900delinsTC	ENSP00000513390.1:n.93+5899_93+5900delins...
ENST00000697666.1:c.140+1735_140+1736delinsTC	ENSP00000513391.1:n.140+1735_140+1736deli...
ENST00000355622.8:c.260+1735_260+1736delinsTC MANE Select	ENSP00000363089.5:n.260+1735_260+1736deli...
ENST00000394487.5:c.140+1735_140+1736delinsTC	ENSP00000377997.4:n.140+1735_140+1736deli...
ENST00000472304.2:c.94-1925_94-1924delinsTC	ENSP00000496429.1:n.94-1925_94-1924delins...
ENST00000642985.1:c.260+1735_260+1736delinsTC	ENSP00000493686.1:n.260+1735_260+1736deli...
ENST00000646089.1:c.93+5899_93+5900delinsTC	ENSP00000496197.1:n.93+5899_93+5900delins...
ENST00000665764.1:c.93+5899_93+5900delinsTC	ENSP00000499745.1:n.93+5899_93+5900delins...
ENST00000355622.6:c.260+1735_260+1736delinsTC	ENSP00000363089.5:n.260+1735_260+1736deli...
ENST00000394487.4:c.140+1735_140+1736delinsTC	ENSP00000377997.4:n.140+1735_140+1736deli...
ENST00000472304.1:n.178-1925_178-1924delinsTC
NM_003266.3:c.140+1735_140+1736delinsTC	NP_003257.1:n.140+1735_140+1736delinsTC
NM_138554.4:c.260+1735_260+1736delinsTC	NP_612564.1:n.260+1735_260+1736delinsTC
NM_138557.2:c.-340-1925_-340-1924delinsTC	NP_612567.1:n.-340-1925_-340-1924delinsTC...
NM_138554.5:c.260+1735_260+1736delinsTC MANE Select	NP_612564.1:n.260+1735_260+1736delinsTC
NM_003266.4:c.140+1735_140+1736delinsTC	NP_003257.1:n.140+1735_140+1736delinsTC
NM_138557.3:c.-340-1925_-340-1924delinsTC	NP_612567.1:n.-340-1925_-340-1924delinsTC...