Canonical Allele Identifier: CA1875353668

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713051C= , CM000671.2:g.117713051C=	GRCh38
NC_000009.11:g.120475329C= , CM000671.1:g.120475329C=	GRCh37
NC_000009.10:g.119515150C=	NCBI36
NG_011475.1:g.13870C=
NG_011475.2:g.13649C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8486C=	ENSP00000496197.1:n.93+8486C=
ENST00000697624.1:n.200+8486C=
ENST00000697625.1:c.93+8486C=	ENSP00000513362.1:n.93+8486C=
ENST00000697636.1:c.93+8486C=	ENSP00000513366.1:n.93+8486C=
ENST00000697637.1:c.93+8486C=	ENSP00000513367.1:n.93+8486C=
ENST00000697664.1:c.140+4322C=	ENSP00000513389.1:n.140+4322C=
ENST00000697665.1:c.93+8486C=	ENSP00000513390.1:n.93+8486C=
ENST00000697666.1:c.140+4322C=	ENSP00000513391.1:n.140+4322C=
ENST00000355622.8:c.923C= MANE Select	ENSP00000363089.5:p.Thr308=
ENST00000394487.5:c.803C=	ENSP00000377997.4:p.Thr268=
ENST00000472304.2:c.*657C=	ENSP00000496429.1:n.*657C=
ENST00000642985.1:c.260+4322C=	ENSP00000493686.1:n.260+4322C=
ENST00000646089.1:c.93+8486C=	ENSP00000496197.1:n.93+8486C=
ENST00000665764.1:c.93+8486C=	ENSP00000499745.1:n.93+8486C=
ENST00000355622.6:c.923C=	ENSP00000363089.5:p.Thr308=
ENST00000394487.4:c.803C=	ENSP00000377997.4:p.Thr268=
ENST00000472304.1:n.840C=
NM_003266.3:c.803C=	NP_003257.1:p.Thr268=
NM_138554.4:c.923C=	NP_612564.1:p.Thr308=
NM_138557.2:c.323C=	NP_612567.1:p.Thr108=
NM_138554.5:c.923C= MANE Select	NP_612564.1:p.Thr308=
NM_003266.4:c.803C=	NP_003257.1:p.Thr268=
NM_138557.3:c.323C=	NP_612567.1:p.Thr108=