Canonical Allele Identifier: CA374655384

Gene: TLR4

Linked Data

• MyVariant Identifiers: chr9:g.120475217A>C (hg19) ; chr9:g.117712939A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117712939A>C , CM000671.2:g.117712939A>C	GRCh38
NC_000009.11:g.120475217A>C , CM000671.1:g.120475217A>C	GRCh37
NC_000009.10:g.119515038A>C	NCBI36
NG_011475.1:g.13758A>C
NG_011475.2:g.13537A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8374A>C	ENSP00000496197.1:n.93+8374A>C
ENST00000697624.1:n.200+8374A>C
ENST00000697625.1:c.93+8374A>C	ENSP00000513362.1:n.93+8374A>C
ENST00000697636.1:c.93+8374A>C	ENSP00000513366.1:n.93+8374A>C
ENST00000697637.1:c.93+8374A>C	ENSP00000513367.1:n.93+8374A>C
ENST00000697664.1:c.140+4210A>C	ENSP00000513389.1:n.140+4210A>C
ENST00000697665.1:c.93+8374A>C	ENSP00000513390.1:n.93+8374A>C
ENST00000697666.1:c.140+4210A>C	ENSP00000513391.1:n.140+4210A>C
ENST00000355622.8:c.811A>C MANE Select	ENSP00000363089.5:p.Lys271Gln
ENST00000394487.5:c.691A>C	ENSP00000377997.4:p.Lys231Gln
ENST00000472304.2:c.*545A>C	ENSP00000496429.1:n.*545A>C
ENST00000642985.1:c.260+4210A>C	ENSP00000493686.1:n.260+4210A>C
ENST00000646089.1:c.93+8374A>C	ENSP00000496197.1:n.93+8374A>C
ENST00000665764.1:c.93+8374A>C	ENSP00000499745.1:n.93+8374A>C
ENST00000355622.6:c.811A>C	ENSP00000363089.5:p.Lys271Gln
ENST00000394487.4:c.691A>C	ENSP00000377997.4:p.Lys231Gln
ENST00000472304.1:n.728A>C
NM_003266.3:c.691A>C	NP_003257.1:p.Lys231Gln
NM_138554.4:c.811A>C	NP_612564.1:p.Lys271Gln
NM_138557.2:c.211A>C	NP_612567.1:p.Lys71Gln
NM_138554.5:c.811A>C MANE Select	NP_612564.1:p.Lys271Gln
NM_003266.4:c.691A>C	NP_003257.1:p.Lys231Gln
NM_138557.3:c.211A>C	NP_612567.1:p.Lys71Gln