Canonical Allele Identifier: CA2691424037

Gene: TLR4

Linked Data

• gnomAD v4: 9-117715784-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117715784G>T , CM000671.2:g.117715784G>T	GRCh38
NC_000009.11:g.120478062G>T , CM000671.1:g.120478062G>T	GRCh37
NC_000009.10:g.119517883G>T	NCBI36
NG_011475.1:g.16603G>T
NG_011475.2:g.16382G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+11219G>T	ENSP00000496197.1:n.93+11219G>T
ENST00000697624.1:n.200+11219G>T
ENST00000697625.1:c.93+11219G>T	ENSP00000513362.1:n.93+11219G>T
ENST00000697636.1:c.93+11219G>T	ENSP00000513366.1:n.93+11219G>T
ENST00000697637.1:c.93+11219G>T	ENSP00000513367.1:n.93+11219G>T
ENST00000697664.1:c.140+7055G>T	ENSP00000513389.1:n.140+7055G>T
ENST00000697665.1:c.93+11219G>T	ENSP00000513390.1:n.93+11219G>T
ENST00000697666.1:c.140+7055G>T	ENSP00000513391.1:n.140+7055G>T
ENST00000355622.8:c.*1136G>T MANE Select	ENSP00000363089.5:n.*1136G>T
ENST00000642985.1:c.260+7055G>T	ENSP00000493686.1:n.260+7055G>T
ENST00000646089.1:c.93+11219G>T	ENSP00000496197.1:n.93+11219G>T
ENST00000665764.1:c.93+11219G>T	ENSP00000499745.1:n.93+11219G>T
ENST00000355622.6:c.*1136G>T	ENSP00000363089.5:n.*1136G>T
NM_003266.3:c.*1136G>T	NP_003257.1:n.*1136G>T
NM_138554.4:c.*1136G>T	NP_612564.1:n.*1136G>T
NM_138557.2:c.*1136G>T	NP_612567.1:n.*1136G>T
NM_138554.5:c.*1136G>T MANE Select	NP_612564.1:n.*1136G>T
NM_003266.4:c.*1136G>T	NP_003257.1:n.*1136G>T
NM_138557.3:c.*1136G>T	NP_612567.1:n.*1136G>T