Canonical Allele Identifier: CA374655418

Gene: TLR4

Linked Data

• MyVariant Identifiers: chr9:g.120475223G>T (hg19) ; chr9:g.117712945G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117712945G>T , CM000671.2:g.117712945G>T	GRCh38
NC_000009.11:g.120475223G>T , CM000671.1:g.120475223G>T	GRCh37
NC_000009.10:g.119515044G>T	NCBI36
NG_011475.1:g.13764G>T
NG_011475.2:g.13543G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+8380G>T	ENSP00000496197.1:n.93+8380G>T
ENST00000697624.1:n.200+8380G>T
ENST00000697625.1:c.93+8380G>T	ENSP00000513362.1:n.93+8380G>T
ENST00000697636.1:c.93+8380G>T	ENSP00000513366.1:n.93+8380G>T
ENST00000697637.1:c.93+8380G>T	ENSP00000513367.1:n.93+8380G>T
ENST00000697664.1:c.140+4216G>T	ENSP00000513389.1:n.140+4216G>T
ENST00000697665.1:c.93+8380G>T	ENSP00000513390.1:n.93+8380G>T
ENST00000697666.1:c.140+4216G>T	ENSP00000513391.1:n.140+4216G>T
ENST00000355622.8:c.817G>T MANE Select	ENSP00000363089.5:p.Asp273Tyr
ENST00000394487.5:c.697G>T	ENSP00000377997.4:p.Asp233Tyr
ENST00000472304.2:c.*551G>T	ENSP00000496429.1:n.*551G>T
ENST00000642985.1:c.260+4216G>T	ENSP00000493686.1:n.260+4216G>T
ENST00000646089.1:c.93+8380G>T	ENSP00000496197.1:n.93+8380G>T
ENST00000665764.1:c.93+8380G>T	ENSP00000499745.1:n.93+8380G>T
ENST00000355622.6:c.817G>T	ENSP00000363089.5:p.Asp273Tyr
ENST00000394487.4:c.697G>T	ENSP00000377997.4:p.Asp233Tyr
ENST00000472304.1:n.734G>T
NM_003266.3:c.697G>T	NP_003257.1:p.Asp233Tyr
NM_138554.4:c.817G>T	NP_612564.1:p.Asp273Tyr
NM_138557.2:c.217G>T	NP_612567.1:p.Asp73Tyr
NM_138554.5:c.817G>T MANE Select	NP_612564.1:p.Asp273Tyr
NM_003266.4:c.697G>T	NP_003257.1:p.Asp233Tyr
NM_138557.3:c.217G>T	NP_612567.1:p.Asp73Tyr