Canonical Allele Identifier: CA1875354024
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117713209A= , CM000671.2:g.117713209A= GRCh38
NC_000009.11:g.120475487A= , CM000671.1:g.120475487A= GRCh37
NC_000009.10:g.119515308A= NCBI36
NG_011475.1:g.14028A=
NG_011475.2:g.13807A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+8644A= ENSP00000496197.1:n.93+8644A=
ENST00000697624.1:n.200+8644A=
ENST00000697625.1:c.93+8644A= ENSP00000513362.1:n.93+8644A=
ENST00000697636.1:c.93+8644A= ENSP00000513366.1:n.93+8644A=
ENST00000697637.1:c.93+8644A= ENSP00000513367.1:n.93+8644A=
ENST00000697664.1:c.140+4480A= ENSP00000513389.1:n.140+4480A=
ENST00000697665.1:c.93+8644A= ENSP00000513390.1:n.93+8644A=
ENST00000697666.1:c.140+4480A= ENSP00000513391.1:n.140+4480A=
ENST00000355622.8:c.1081A= MANE Select ENSP00000363089.5:p.Asn361=
ENST00000394487.5:c.961A= ENSP00000377997.4:p.Asn321=
ENST00000472304.2:c.*815A= ENSP00000496429.1:n.*815A=
ENST00000642985.1:c.260+4480A= ENSP00000493686.1:n.260+4480A=
ENST00000646089.1:c.93+8644A= ENSP00000496197.1:n.93+8644A=
ENST00000665764.1:c.93+8644A= ENSP00000499745.1:n.93+8644A=
ENST00000355622.6:c.1081A= ENSP00000363089.5:p.Asn361=
ENST00000394487.4:c.961A= ENSP00000377997.4:p.Asn321=
ENST00000472304.1:n.998A=
NM_003266.3:c.961A= NP_003257.1:p.Asn321=
NM_138554.4:c.1081A= NP_612564.1:p.Asn361=
NM_138557.2:c.481A= NP_612567.1:p.Asn161=
NM_138554.5:c.1081A= MANE Select NP_612564.1:p.Asn361=
NM_003266.4:c.961A= NP_003257.1:p.Asn321=
NM_138557.3:c.481A= NP_612567.1:p.Asn161=