Canonical Allele Identifier: CA1875358379

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117707570G= , CM000671.2:g.117707570G=	GRCh38
NC_000009.11:g.120469848G= , CM000671.1:g.120469848G=	GRCh37
NC_000009.10:g.119509669G=	NCBI36
NG_011475.1:g.8389G=
NG_011475.2:g.8168G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+3005G=	ENSP00000496197.1:n.93+3005G=
ENST00000697624.1:n.200+3005G=
ENST00000697625.1:c.93+3005G=	ENSP00000513362.1:n.93+3005G=
ENST00000697636.1:c.93+3005G=	ENSP00000513366.1:n.93+3005G=
ENST00000697637.1:c.93+3005G=	ENSP00000513367.1:n.93+3005G=
ENST00000697664.1:c.-147-629G=	ENSP00000513389.1:n.-147-629G=
ENST00000697665.1:c.93+3005G=	ENSP00000513390.1:n.93+3005G=
ENST00000697666.1:c.-147-629G=	ENSP00000513391.1:n.-147-629G=
ENST00000355622.8:c.94-993G= MANE Select	ENSP00000363089.5:n.94-993G=
ENST00000394487.5:c.-147-629G=	ENSP00000377997.4:n.-147-629G=
ENST00000472304.2:c.93+3005G=	ENSP00000496429.1:n.93+3005G=
ENST00000642985.1:c.94-993G=	ENSP00000493686.1:n.94-993G=
ENST00000646089.1:c.93+3005G=	ENSP00000496197.1:n.93+3005G=
ENST00000665764.1:c.93+3005G=	ENSP00000499745.1:n.93+3005G=
ENST00000355622.6:c.94-993G=	ENSP00000363089.5:n.94-993G=
ENST00000394487.4:c.-147-629G=	ENSP00000377997.4:n.-147-629G=
ENST00000472304.1:n.177+3005G=
NM_003266.3:c.-147-629G=	NP_003257.1:n.-147-629G=
NM_138554.4:c.94-993G=	NP_612564.1:n.94-993G=
NM_138557.2:c.-341+3005G=	NP_612567.1:n.-341+3005G=
NM_138554.5:c.94-993G= MANE Select	NP_612564.1:n.94-993G=
NM_003266.4:c.-147-629G=	NP_003257.1:n.-147-629G=
NM_138557.3:c.-341+3005G=	NP_612567.1:n.-341+3005G=