Canonical Allele Identifier: CA2691424818

Gene: TLR4

Linked Data

• gnomAD v4: 9-117718542-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718542T>C , CM000671.2:g.117718542T>C	GRCh38
NC_000009.11:g.120480820T>C , CM000671.1:g.120480820T>C	GRCh37
NC_000009.10:g.119520641T>C	NCBI36
NG_011475.1:g.19361T>C
NG_011475.2:g.19140T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+13977T>C	ENSP00000496197.1:n.93+13977T>C
ENST00000697624.1:n.200+13977T>C
ENST00000697625.1:c.93+13977T>C	ENSP00000513362.1:n.93+13977T>C
ENST00000697636.1:c.93+13977T>C	ENSP00000513366.1:n.93+13977T>C
ENST00000697637.1:c.93+13977T>C	ENSP00000513367.1:n.93+13977T>C
ENST00000697664.1:c.140+9813T>C	ENSP00000513389.1:n.140+9813T>C
ENST00000697665.1:c.93+13977T>C	ENSP00000513390.1:n.93+13977T>C
ENST00000697666.1:c.140+9813T>C	ENSP00000513391.1:n.140+9813T>C
ENST00000355622.8:c.*3894T>C MANE Select	ENSP00000363089.5:n.*3894T>C
ENST00000642985.1:c.260+9813T>C	ENSP00000493686.1:n.260+9813T>C
ENST00000646089.1:c.93+13977T>C	ENSP00000496197.1:n.93+13977T>C
ENST00000665764.1:c.93+13977T>C	ENSP00000499745.1:n.93+13977T>C
NM_138554.5:c.*3894T>C MANE Select	NP_612564.1:n.*3894T>C
NM_003266.4:c.*3894T>C	NP_003257.1:n.*3894T>C
NM_138557.3:c.*3894T>C	NP_612567.1:n.*3894T>C