Canonical Allele Identifier: CA1875361484
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117718537A= , CM000671.2:g.117718537A= GRCh38
NC_000009.11:g.120480815A= , CM000671.1:g.120480815A= GRCh37
NC_000009.10:g.119520636A= NCBI36
NG_011475.1:g.19356A=
NG_011475.2:g.19135A=

Transcript Alleles

HGVS Amino-acid change
ENST00000646089.2:c.93+13972A= ENSP00000496197.1:n.93+13972A=
ENST00000697624.1:n.200+13972A=
ENST00000697625.1:c.93+13972A= ENSP00000513362.1:n.93+13972A=
ENST00000697636.1:c.93+13972A= ENSP00000513366.1:n.93+13972A=
ENST00000697637.1:c.93+13972A= ENSP00000513367.1:n.93+13972A=
ENST00000697664.1:c.140+9808A= ENSP00000513389.1:n.140+9808A=
ENST00000697665.1:c.93+13972A= ENSP00000513390.1:n.93+13972A=
ENST00000697666.1:c.140+9808A= ENSP00000513391.1:n.140+9808A=
ENST00000355622.8:c.*3889A= MANE Select ENSP00000363089.5:n.*3889A=
ENST00000642985.1:c.260+9808A= ENSP00000493686.1:n.260+9808A=
ENST00000646089.1:c.93+13972A= ENSP00000496197.1:n.93+13972A=
ENST00000665764.1:c.93+13972A= ENSP00000499745.1:n.93+13972A=
NM_138554.5:c.*3889A= MANE Select NP_612564.1:n.*3889A=
NM_003266.4:c.*3889A= NP_003257.1:n.*3889A=
NM_138557.3:c.*3889A= NP_612567.1:n.*3889A=