Canonical Allele Identifier: CA1875354037

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713211C= , CM000671.2:g.117713211C=	GRCh38
NC_000009.11:g.120475489C= , CM000671.1:g.120475489C=	GRCh37
NC_000009.10:g.119515310C=	NCBI36
NG_011475.1:g.14030C=
NG_011475.2:g.13809C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8646C=	ENSP00000496197.1:n.93+8646C=
ENST00000697624.1:n.200+8646C=
ENST00000697625.1:c.93+8646C=	ENSP00000513362.1:n.93+8646C=
ENST00000697636.1:c.93+8646C=	ENSP00000513366.1:n.93+8646C=
ENST00000697637.1:c.93+8646C=	ENSP00000513367.1:n.93+8646C=
ENST00000697664.1:c.140+4482C=	ENSP00000513389.1:n.140+4482C=
ENST00000697665.1:c.93+8646C=	ENSP00000513390.1:n.93+8646C=
ENST00000697666.1:c.140+4482C=	ENSP00000513391.1:n.140+4482C=
ENST00000355622.8:c.1083C= MANE Select	ENSP00000363089.5:p.Asn361=
ENST00000394487.5:c.963C=	ENSP00000377997.4:p.Asn321=
ENST00000472304.2:c.*817C=	ENSP00000496429.1:n.*817C=
ENST00000642985.1:c.260+4482C=	ENSP00000493686.1:n.260+4482C=
ENST00000646089.1:c.93+8646C=	ENSP00000496197.1:n.93+8646C=
ENST00000665764.1:c.93+8646C=	ENSP00000499745.1:n.93+8646C=
ENST00000355622.6:c.1083C=	ENSP00000363089.5:p.Asn361=
ENST00000394487.4:c.963C=	ENSP00000377997.4:p.Asn321=
ENST00000472304.1:n.1000C=
NM_003266.3:c.963C=	NP_003257.1:p.Asn321=
NM_138554.4:c.1083C=	NP_612564.1:p.Asn361=
NM_138557.2:c.483C=	NP_612567.1:p.Asn161=
NM_138554.5:c.1083C= MANE Select	NP_612564.1:p.Asn361=
NM_003266.4:c.963C=	NP_003257.1:p.Asn321=
NM_138557.3:c.483C=	NP_612567.1:p.Asn161=