Canonical Allele Identifier: CA859281620

Gene: TLR4

Linked Data

• dbSNP Id: rs1388233666
• gnomAD v3: 9-117709751-CCTATTATA-C
• gnomAD v4: 9-117709751-CCTATTATA-C
• MyVariant Identifiers: chr9:g.120472030_120472037del (hg19) ; chr9:g.117709752_117709759del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117709754_117709761del , CM000671.2:g.117709754_117709761del	GRCh38
NC_000009.11:g.120472032_120472039del , CM000671.1:g.120472032_120472039del	GRCh37
NC_000009.10:g.119511853_119511860del	NCBI36
NG_011475.1:g.10573_10580del
NG_011475.2:g.10352_10359del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+5189_93+5196del	ENSP00000496197.1:n.93+5189_93+5196del
ENST00000697624.1:n.200+5189_200+5196del
ENST00000697625.1:c.93+5189_93+5196del	ENSP00000513362.1:n.93+5189_93+5196del
ENST00000697636.1:c.93+5189_93+5196del	ENSP00000513366.1:n.93+5189_93+5196del
ENST00000697637.1:c.93+5189_93+5196del	ENSP00000513367.1:n.93+5189_93+5196del
ENST00000697664.1:c.140+1025_140+1032del	ENSP00000513389.1:n.140+1025_140+1032del
ENST00000697665.1:c.93+5189_93+5196del	ENSP00000513390.1:n.93+5189_93+5196del
ENST00000697666.1:c.140+1025_140+1032del	ENSP00000513391.1:n.140+1025_140+1032del
ENST00000355622.8:c.260+1025_260+1032del MANE Select	ENSP00000363089.5:n.260+1025_260+1032del
ENST00000394487.5:c.140+1025_140+1032del	ENSP00000377997.4:n.140+1025_140+1032del
ENST00000472304.2:c.94-2635_94-2628del	ENSP00000496429.1:n.94-2635_94-2628del
ENST00000642985.1:c.260+1025_260+1032del	ENSP00000493686.1:n.260+1025_260+1032del
ENST00000646089.1:c.93+5189_93+5196del	ENSP00000496197.1:n.93+5189_93+5196del
ENST00000665764.1:c.93+5189_93+5196del	ENSP00000499745.1:n.93+5189_93+5196del
ENST00000355622.6:c.260+1025_260+1032del	ENSP00000363089.5:n.260+1025_260+1032del
ENST00000394487.4:c.140+1025_140+1032del	ENSP00000377997.4:n.140+1025_140+1032del
ENST00000472304.1:n.178-2635_178-2628del
NM_003266.3:c.140+1025_140+1032del	NP_003257.1:n.140+1025_140+1032del
NM_138554.4:c.260+1025_260+1032del	NP_612564.1:n.260+1025_260+1032del
NM_138557.2:c.-340-2635_-340-2628del	NP_612567.1:n.-340-2635_-340-2628del
NM_138554.5:c.260+1025_260+1032del MANE Select	NP_612564.1:n.260+1025_260+1032del
NM_003266.4:c.140+1025_140+1032del	NP_003257.1:n.140+1025_140+1032del
NM_138557.3:c.-340-2635_-340-2628del	NP_612567.1:n.-340-2635_-340-2628del