Canonical Allele Identifier: CA1875351830

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117712004G= , CM000671.2:g.117712004G=	GRCh38
NC_000009.11:g.120474282G= , CM000671.1:g.120474282G=	GRCh37
NC_000009.10:g.119514103G=	NCBI36
NG_011475.1:g.12823G=
NG_011475.2:g.12602G=

Transcript Alleles

HGVS	Amino-acid Change
NM_138554.5:c.261-385G= MANE Select	NP_612564.1:n.261-385G=
ENST00000355622.8:c.261-385G= MANE Select	ENSP00000363089.5:n.261-385G=
NM_003266.3:c.141-385G=	NP_003257.1:n.141-385G=
NM_003266.4:c.141-385G=	NP_003257.1:n.141-385G=
NM_138554.4:c.261-385G=	NP_612564.1:n.261-385G=
NM_138557.2:c.-340-385G=	NP_612567.1:n.-340-385G=
NM_138557.3:c.-340-385G=	NP_612567.1:n.-340-385G=
ENST00000355622.6:c.261-385G=	ENSP00000363089.5:n.261-385G=
ENST00000394487.4:c.141-385G=	ENSP00000377997.4:n.141-385G=
ENST00000394487.5:c.141-385G=	ENSP00000377997.4:n.141-385G=
ENST00000472304.1:n.178-385G=
ENST00000472304.2:c.94-385G=	ENSP00000496429.1:n.94-385G=
ENST00000642985.1:c.260+3275G=	ENSP00000493686.1:n.260+3275G=
ENST00000646089.1:c.93+7439G=	ENSP00000496197.1:n.93+7439G=
ENST00000646089.2:c.93+7439G=	ENSP00000496197.1:n.93+7439G=
ENST00000665764.1:c.93+7439G=	ENSP00000499745.1:n.93+7439G=
ENST00000697624.1:n.200+7439G=
ENST00000697625.1:c.93+7439G=	ENSP00000513362.1:n.93+7439G=
ENST00000697636.1:c.93+7439G=	ENSP00000513366.1:n.93+7439G=
ENST00000697637.1:c.93+7439G=	ENSP00000513367.1:n.93+7439G=
ENST00000697664.1:c.140+3275G=	ENSP00000513389.1:n.140+3275G=
ENST00000697665.1:c.93+7439G=	ENSP00000513390.1:n.93+7439G=
ENST00000697666.1:c.140+3275G=	ENSP00000513391.1:n.140+3275G=