Canonical Allele Identifier: CA1875358262

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117707457G= , CM000671.2:g.117707457G=	GRCh38
NC_000009.11:g.120469735G= , CM000671.1:g.120469735G=	GRCh37
NC_000009.10:g.119509556G=	NCBI36
NG_011475.1:g.8276G=
NG_011475.2:g.8055G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646089.2:c.93+2892G=	ENSP00000496197.1:n.93+2892G=
ENST00000697624.1:n.200+2892G=
ENST00000697625.1:c.93+2892G=	ENSP00000513362.1:n.93+2892G=
ENST00000697636.1:c.93+2892G=	ENSP00000513366.1:n.93+2892G=
ENST00000697637.1:c.93+2892G=	ENSP00000513367.1:n.93+2892G=
ENST00000697664.1:c.-147-742G=	ENSP00000513389.1:n.-147-742G=
ENST00000697665.1:c.93+2892G=	ENSP00000513390.1:n.93+2892G=
ENST00000697666.1:c.-147-742G=	ENSP00000513391.1:n.-147-742G=
ENST00000355622.8:c.94-1106G= MANE Select	ENSP00000363089.5:n.94-1106G=
ENST00000394487.5:c.-147-742G=	ENSP00000377997.4:n.-147-742G=
ENST00000472304.2:c.93+2892G=	ENSP00000496429.1:n.93+2892G=
ENST00000642985.1:c.94-1106G=	ENSP00000493686.1:n.94-1106G=
ENST00000646089.1:c.93+2892G=	ENSP00000496197.1:n.93+2892G=
ENST00000665764.1:c.93+2892G=	ENSP00000499745.1:n.93+2892G=
ENST00000355622.6:c.94-1106G=	ENSP00000363089.5:n.94-1106G=
ENST00000394487.4:c.-147-742G=	ENSP00000377997.4:n.-147-742G=
ENST00000472304.1:n.177+2892G=
NM_003266.3:c.-147-742G=	NP_003257.1:n.-147-742G=
NM_138554.4:c.94-1106G=	NP_612564.1:n.94-1106G=
NM_138557.2:c.-341+2892G=	NP_612567.1:n.-341+2892G=
NM_138554.5:c.94-1106G= MANE Select	NP_612564.1:n.94-1106G=
NM_003266.4:c.-147-742G=	NP_003257.1:n.-147-742G=
NM_138557.3:c.-341+2892G=	NP_612567.1:n.-341+2892G=