Canonical Allele Identifier: CA467037470

Gene: TLR4

Linked Data

• MyVariant Identifiers: chr9:g.120475876_120475877insTCCCCGCGGGGA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713598_117713599insTCCCCGCGGGGA , CM000671.2:g.117713598_117713599insTCCCCGCGGGGA	GRCh38
NC_000009.11:g.120475876_120475877insTCCCCGCGGGGA , CM000671.1:g.120475876_120475877insTCCCCGCGGGGA	GRCh37
NC_000009.10:g.119515697_119515698insTCCCCGCGGGGA	NCBI36
NG_011475.1:g.14417_14418insTCCCCGCGGGGA
NG_011475.2:g.14196_14197insTCCCCGCGGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9033_93+9034insTCCCCGCGGGGA	ENSP00000496197.1:n.93+9033_93+9034insTCCCCGCGGGGA
ENST00000697624.1:n.200+9033_200+9034insTCCCCGCGGGGA
ENST00000697625.1:c.93+9033_93+9034insTCCCCGCGGGGA	ENSP00000513362.1:n.93+9033_93+9034insTCCCCGCGGGGA
ENST00000697636.1:c.93+9033_93+9034insTCCCCGCGGGGA	ENSP00000513366.1:n.93+9033_93+9034insTCCCCGCGGGGA
ENST00000697637.1:c.93+9033_93+9034insTCCCCGCGGGGA	ENSP00000513367.1:n.93+9033_93+9034insTCCCCGCGGGGA
ENST00000697664.1:c.140+4869_140+4870insTCCCCGCGGGGA	ENSP00000513389.1:n.140+4869_140+4870insTCCCCGCGGGGA
ENST00000697665.1:c.93+9033_93+9034insTCCCCGCGGGGA	ENSP00000513390.1:n.93+9033_93+9034insTCCCCGCGGGGA
ENST00000697666.1:c.140+4869_140+4870insTCCCCGCGGGGA	ENSP00000513391.1:n.140+4869_140+4870insTCCCCGCGGGGA
ENST00000355622.8:c.1470_1471insTCCCCGCGGGGA MANE Select	ENSP00000363089.5:p.Asp490_Ile491insSerProArgGly
ENST00000394487.5:c.1350_1351insTCCCCGCGGGGA	ENSP00000377997.4:p.Asp450_Ile451insSerProArgGly
ENST00000472304.2:c.*1204_*1205insTCCCCGCGGGGA	ENSP00000496429.1:n.*1204_*1205insTCCCCGCGGGGA
ENST00000642985.1:c.260+4869_260+4870insTCCCCGCGGGGA	ENSP00000493686.1:n.260+4869_260+4870insTCCCCGCGGGGA
ENST00000646089.1:c.93+9033_93+9034insTCCCCGCGGGGA	ENSP00000496197.1:n.93+9033_93+9034insTCCCCGCGGGGA
ENST00000665764.1:c.93+9033_93+9034insTCCCCGCGGGGA	ENSP00000499745.1:n.93+9033_93+9034insTCCCCGCGGGGA
ENST00000355622.6:c.1470_1471insTCCCCGCGGGGA	ENSP00000363089.5:p.Asp490_Ile491insSerProArgGly
ENST00000394487.4:c.1350_1351insTCCCCGCGGGGA	ENSP00000377997.4:p.Asp450_Ile451insSerProArgGly
ENST00000472304.1:n.1387_1388insTCCCCGCGGGGA
NM_003266.3:c.1350_1351insTCCCCGCGGGGA	NP_003257.1:p.Asp450_Ile451insSerProArgGly
NM_138554.4:c.1470_1471insTCCCCGCGGGGA	NP_612564.1:p.Asp490_Ile491insSerProArgGly
NM_138557.2:c.870_871insTCCCCGCGGGGA	NP_612567.1:p.Asp290_Ile291insSerProArgGly
NM_138554.5:c.1470_1471insTCCCCGCGGGGA MANE Select	NP_612564.1:p.Asp490_Ile491insSerProArgGly
NM_003266.4:c.1350_1351insTCCCCGCGGGGA	NP_003257.1:p.Asp450_Ile451insSerProArgGly
NM_138557.3:c.870_871insTCCCCGCGGGGA	NP_612567.1:p.Asp290_Ile291insSerProArgGly