Canonical Allele Identifier: CA1875353645
Gene: TLR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117713041A= , CM000671.2:g.117713041A= GRCh38
NC_000009.11:g.120475319A= , CM000671.1:g.120475319A= GRCh37
NC_000009.10:g.119515140A= NCBI36
NG_011475.1:g.13860A=
NG_011475.2:g.13639A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.93+8476A= ENSP00000496197.1:n.93+8476A=
ENST00000697624.1:n.200+8476A=
ENST00000697625.1:c.93+8476A= ENSP00000513362.1:n.93+8476A=
ENST00000697636.1:c.93+8476A= ENSP00000513366.1:n.93+8476A=
ENST00000697637.1:c.93+8476A= ENSP00000513367.1:n.93+8476A=
ENST00000697664.1:c.140+4312A= ENSP00000513389.1:n.140+4312A=
ENST00000697665.1:c.93+8476A= ENSP00000513390.1:n.93+8476A=
ENST00000697666.1:c.140+4312A= ENSP00000513391.1:n.140+4312A=
ENST00000355622.8:c.913A= MANE Select ENSP00000363089.5:p.Asn305=
ENST00000394487.5:c.793A= ENSP00000377997.4:p.Asn265=
ENST00000472304.2:c.*647A= ENSP00000496429.1:n.*647A=
ENST00000642985.1:c.260+4312A= ENSP00000493686.1:n.260+4312A=
ENST00000646089.1:c.93+8476A= ENSP00000496197.1:n.93+8476A=
ENST00000665764.1:c.93+8476A= ENSP00000499745.1:n.93+8476A=
ENST00000355622.6:c.913A= ENSP00000363089.5:p.Asn305=
ENST00000394487.4:c.793A= ENSP00000377997.4:p.Asn265=
ENST00000472304.1:n.830A=
NM_003266.3:c.793A= NP_003257.1:p.Asn265=
NM_138554.4:c.913A= NP_612564.1:p.Asn305=
NM_138557.2:c.313A= NP_612567.1:p.Asn105=
NM_138554.5:c.913A= MANE Select NP_612564.1:p.Asn305=
NM_003266.4:c.793A= NP_003257.1:p.Asn265=
NM_138557.3:c.313A= NP_612567.1:p.Asn105=