Canonical Allele Identifier: CA1875354547

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713547C= , CM000671.2:g.117713547C=	GRCh38
NC_000009.11:g.120475825C= , CM000671.1:g.120475825C=	GRCh37
NC_000009.10:g.119515646C=	NCBI36
NG_011475.1:g.14366C=
NG_011475.2:g.14145C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8982C=	ENSP00000496197.1:n.93+8982C=
ENST00000697624.1:n.200+8982C=
ENST00000697625.1:c.93+8982C=	ENSP00000513362.1:n.93+8982C=
ENST00000697636.1:c.93+8982C=	ENSP00000513366.1:n.93+8982C=
ENST00000697637.1:c.93+8982C=	ENSP00000513367.1:n.93+8982C=
ENST00000697664.1:c.140+4818C=	ENSP00000513389.1:n.140+4818C=
ENST00000697665.1:c.93+8982C=	ENSP00000513390.1:n.93+8982C=
ENST00000697666.1:c.140+4818C=	ENSP00000513391.1:n.140+4818C=
ENST00000355622.8:c.1419C= MANE Select	ENSP00000363089.5:p.Leu473=
ENST00000394487.5:c.1299C=	ENSP00000377997.4:p.Leu433=
ENST00000472304.2:c.*1153C=	ENSP00000496429.1:n.*1153C=
ENST00000642985.1:c.260+4818C=	ENSP00000493686.1:n.260+4818C=
ENST00000646089.1:c.93+8982C=	ENSP00000496197.1:n.93+8982C=
ENST00000665764.1:c.93+8982C=	ENSP00000499745.1:n.93+8982C=
ENST00000355622.6:c.1419C=	ENSP00000363089.5:p.Leu473=
ENST00000394487.4:c.1299C=	ENSP00000377997.4:p.Leu433=
ENST00000472304.1:n.1336C=
NM_003266.3:c.1299C=	NP_003257.1:p.Leu433=
NM_138554.4:c.1419C=	NP_612564.1:p.Leu473=
NM_138557.2:c.819C=	NP_612567.1:p.Leu273=
NM_138554.5:c.1419C= MANE Select	NP_612564.1:p.Leu473=
NM_003266.4:c.1299C=	NP_003257.1:p.Leu433=
NM_138557.3:c.819C=	NP_612567.1:p.Leu273=