Canonical Allele Identifier: CA344694756
Gene: TLR5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.223112151T>A , CM000663.2:g.223112151T>A GRCh38
NC_000001.10:g.223285493T>A , CM000663.1:g.223285493T>A GRCh37
NC_000001.9:g.221352116T>A NCBI36
NG_016244.1:g.36132A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000642603.2:c.881A>T MANE Select ENSP00000496355.1:p.Asp294Val
ENST00000645434.1:c.881A>T ENSP00000493892.1:p.Asp294Val
ENST00000366881.5:c.881A>T ENSP00000355846.1:p.Asp294Val
ENST00000540964.5:c.881A>T ENSP00000440643.1:p.Asp294Val
NM_003268.5:c.881A>T NP_003259.2:p.Asp294Val
XM_005273241.3:c.881A>T XP_005273298.2:p.Asp294Val
XM_005273242.3:c.881A>T XP_005273299.2:p.Asp294Val
XM_005273243.3:c.881A>T XP_005273300.2:p.Asp294Val
XM_006711504.2:c.881A>T XP_006711567.1:p.Asp294Val
XM_006711505.2:c.881A>T XP_006711568.1:p.Asp294Val
XM_006711506.2:c.881A>T XP_006711569.1:p.Asp294Val
XM_011509937.1:c.881A>T XP_011508239.1:p.Asp294Val
XM_005273241.4:c.881A>T XP_005273298.2:p.Asp294Val
XM_005273242.4:c.881A>T XP_005273299.2:p.Asp294Val
XM_005273243.4:c.881A>T XP_005273300.2:p.Asp294Val
XM_006711504.3:c.881A>T XP_006711567.1:p.Asp294Val
XM_006711505.3:c.881A>T XP_006711568.1:p.Asp294Val
XM_006711506.3:c.881A>T XP_006711569.1:p.Asp294Val
XM_011509937.2:c.881A>T XP_011508239.1:p.Asp294Val
XM_017002208.1:c.881A>T XP_016857697.1:p.Asp294Val
NM_003268.6:c.881A>T MANE Select NP_003259.2:p.Asp294Val