Canonical Allele Identifier: CA1875354906

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713776_117713778delinsGAT , CM000671.2:g.117713776_117713778delinsGAT	GRCh38
NC_000009.11:g.120476054_120476056delinsGAT , CM000671.1:g.120476054_120476056delinsGAT	GRCh37
NC_000009.10:g.119515875_119515877delinsGAT	NCBI36
NG_011475.1:g.14595_14597delinsGAT
NG_011475.2:g.14374_14376delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9211_93+9213delinsGAT	ENSP00000496197.1:n.93+9211_93+9213delinsGAT
ENST00000697624.1:n.200+9211_200+9213delinsGAT
ENST00000697625.1:c.93+9211_93+9213delinsGAT	ENSP00000513362.1:n.93+9211_93+9213delinsGAT
ENST00000697636.1:c.93+9211_93+9213delinsGAT	ENSP00000513366.1:n.93+9211_93+9213delinsGAT
ENST00000697637.1:c.93+9211_93+9213delinsGAT	ENSP00000513367.1:n.93+9211_93+9213delinsGAT
ENST00000697664.1:c.140+5047_140+5049delinsGAT	ENSP00000513389.1:n.140+5047_140+5049delinsGAT
ENST00000697665.1:c.93+9211_93+9213delinsGAT	ENSP00000513390.1:n.93+9211_93+9213delinsGAT
ENST00000697666.1:c.140+5047_140+5049delinsGAT	ENSP00000513391.1:n.140+5047_140+5049delinsGAT
ENST00000355622.8:c.1648_1650delinsGAT MANE Select	ENSP00000363089.5:p.Asp550=
ENST00000394487.5:c.1528_1530delinsGAT	ENSP00000377997.4:p.Asp510=
ENST00000472304.2:c.*1382_*1384delinsGAT	ENSP00000496429.1:n.*1382_*1384delinsGAT
ENST00000642985.1:c.260+5047_260+5049delinsGAT	ENSP00000493686.1:n.260+5047_260+5049delinsGAT
ENST00000646089.1:c.93+9211_93+9213delinsGAT	ENSP00000496197.1:n.93+9211_93+9213delinsGAT
ENST00000665764.1:c.93+9211_93+9213delinsGAT	ENSP00000499745.1:n.93+9211_93+9213delinsGAT
ENST00000355622.6:c.1648_1650delinsGAT	ENSP00000363089.5:p.Asp550=
ENST00000394487.4:c.1528_1530delinsGAT	ENSP00000377997.4:p.Asp510=
ENST00000472304.1:n.1565_1567delinsGAT
NM_003266.3:c.1528_1530delinsGAT	NP_003257.1:p.Asp510=
NM_138554.4:c.1648_1650delinsGAT	NP_612564.1:p.Asp550=
NM_138557.2:c.1048_1050delinsGAT	NP_612567.1:p.Asp350=
NM_138554.5:c.1648_1650delinsGAT MANE Select	NP_612564.1:p.Asp550=
NM_003266.4:c.1528_1530delinsGAT	NP_003257.1:p.Asp510=
NM_138557.3:c.1048_1050delinsGAT	NP_612567.1:p.Asp350=