Canonical Allele Identifier: CA374656493

Gene: TLR4

Linked Data

• MyVariant Identifiers: chr9:g.120475662T>C (hg19) ; chr9:g.117713384T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713384T>C , CM000671.2:g.117713384T>C	GRCh38
NC_000009.11:g.120475662T>C , CM000671.1:g.120475662T>C	GRCh37
NC_000009.10:g.119515483T>C	NCBI36
NG_011475.1:g.14203T>C
NG_011475.2:g.13982T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8819T>C	ENSP00000496197.1:n.93+8819T>C
ENST00000697624.1:n.200+8819T>C
ENST00000697625.1:c.93+8819T>C	ENSP00000513362.1:n.93+8819T>C
ENST00000697636.1:c.93+8819T>C	ENSP00000513366.1:n.93+8819T>C
ENST00000697637.1:c.93+8819T>C	ENSP00000513367.1:n.93+8819T>C
ENST00000697664.1:c.140+4655T>C	ENSP00000513389.1:n.140+4655T>C
ENST00000697665.1:c.93+8819T>C	ENSP00000513390.1:n.93+8819T>C
ENST00000697666.1:c.140+4655T>C	ENSP00000513391.1:n.140+4655T>C
ENST00000355622.8:c.1256T>C MANE Select	ENSP00000363089.5:p.Leu419Ser
ENST00000394487.5:c.1136T>C	ENSP00000377997.4:p.Leu379Ser
ENST00000472304.2:c.*990T>C	ENSP00000496429.1:n.*990T>C
ENST00000642985.1:c.260+4655T>C	ENSP00000493686.1:n.260+4655T>C
ENST00000646089.1:c.93+8819T>C	ENSP00000496197.1:n.93+8819T>C
ENST00000665764.1:c.93+8819T>C	ENSP00000499745.1:n.93+8819T>C
ENST00000355622.6:c.1256T>C	ENSP00000363089.5:p.Leu419Ser
ENST00000394487.4:c.1136T>C	ENSP00000377997.4:p.Leu379Ser
ENST00000472304.1:n.1173T>C
NM_003266.3:c.1136T>C	NP_003257.1:p.Leu379Ser
NM_138554.4:c.1256T>C	NP_612564.1:p.Leu419Ser
NM_138557.2:c.656T>C	NP_612567.1:p.Leu219Ser
NM_138554.5:c.1256T>C MANE Select	NP_612564.1:p.Leu419Ser
NM_003266.4:c.1136T>C	NP_003257.1:p.Leu379Ser
NM_138557.3:c.656T>C	NP_612567.1:p.Leu219Ser