Canonical Allele Identifier: CA1148297573

Gene: TLR5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.223112143G= , CM000663.2:g.223112143G=	GRCh38
NC_000001.10:g.223285485G= , CM000663.1:g.223285485G=	GRCh37
NC_000001.9:g.221352108G=	NCBI36
NG_016244.1:g.36140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642603.2:c.889C= MANE Select	ENSP00000496355.1:p.His297=
ENST00000645434.1:c.889C=	ENSP00000493892.1:p.His297=
ENST00000366881.5:c.889C=	ENSP00000355846.1:p.His297=
ENST00000540964.5:c.889C=	ENSP00000440643.1:p.His297=
NM_003268.5:c.889C=	NP_003259.2:p.His297=
XM_005273241.3:c.889C=	XP_005273298.2:p.His297=
XM_005273242.3:c.889C=	XP_005273299.2:p.His297=
XM_005273243.3:c.889C=	XP_005273300.2:p.His297=
XM_006711504.2:c.889C=	XP_006711567.1:p.His297=
XM_006711505.2:c.889C=	XP_006711568.1:p.His297=
XM_006711506.2:c.889C=	XP_006711569.1:p.His297=
XM_011509937.1:c.889C=	XP_011508239.1:p.His297=
XM_005273241.4:c.889C=	XP_005273298.2:p.His297=
XM_005273242.4:c.889C=	XP_005273299.2:p.His297=
XM_005273243.4:c.889C=	XP_005273300.2:p.His297=
XM_006711504.3:c.889C=	XP_006711567.1:p.His297=
XM_006711505.3:c.889C=	XP_006711568.1:p.His297=
XM_006711506.3:c.889C=	XP_006711569.1:p.His297=
XM_011509937.2:c.889C=	XP_011508239.1:p.His297=
XM_017002208.1:c.889C=	XP_016857697.1:p.His297=
NM_003268.6:c.889C= MANE Select	NP_003259.2:p.His297=