Canonical Allele Identifier: CA2785737339

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117718579G>A , CM000671.2:g.117718579G>A	GRCh38
NC_000009.11:g.120480857G>A , CM000671.1:g.120480857G>A	GRCh37
NC_000009.10:g.119520678G>A	NCBI36
NG_011475.1:g.19398G>A
NG_011475.2:g.19177G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+14014G>A	ENSP00000496197.1:n.93+14014G>A
ENST00000697624.1:n.200+14014G>A
ENST00000697625.1:c.93+14014G>A	ENSP00000513362.1:n.93+14014G>A
ENST00000697636.1:c.93+14014G>A	ENSP00000513366.1:n.93+14014G>A
ENST00000697637.1:c.93+14014G>A	ENSP00000513367.1:n.93+14014G>A
ENST00000697664.1:c.140+9850G>A	ENSP00000513389.1:n.140+9850G>A
ENST00000697665.1:c.93+14014G>A	ENSP00000513390.1:n.93+14014G>A
ENST00000697666.1:c.140+9850G>A	ENSP00000513391.1:n.140+9850G>A
ENST00000355622.8:c.*3931G>A MANE Select	ENSP00000363089.5:n.*3931G>A
ENST00000642985.1:c.260+9850G>A	ENSP00000493686.1:n.260+9850G>A
ENST00000646089.1:c.93+14014G>A	ENSP00000496197.1:n.93+14014G>A
ENST00000665764.1:c.93+14014G>A	ENSP00000499745.1:n.93+14014G>A
NM_138554.5:c.*3931G>A MANE Select	NP_612564.1:n.*3931G>A
NM_003266.4:c.*3931G>A	NP_003257.1:n.*3931G>A
NM_138557.3:c.*3931G>A	NP_612567.1:n.*3931G>A