Canonical Allele Identifier: CA423724606

Gene: TLR5

Linked Data

• MyVariant Identifiers: chr1:g.223285378A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.223112036A>G , CM000663.2:g.223112036A>G	GRCh38
NC_000001.10:g.223285378A>G , CM000663.1:g.223285378A>G	GRCh37
NC_000001.9:g.221352001A>G	NCBI36
NG_016244.1:g.36247T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642603.2:c.996T>C MANE Select	ENSP00000496355.1:p.Phe332=
ENST00000645434.1:c.996T>C	ENSP00000493892.1:p.Phe332=
ENST00000366881.5:c.996T>C	ENSP00000355846.1:p.Phe332=
ENST00000540964.5:c.996T>C	ENSP00000440643.1:p.Phe332=
NM_003268.5:c.996T>C	NP_003259.2:p.Phe332=
XM_005273241.3:c.996T>C	XP_005273298.2:p.Phe332=
XM_005273242.3:c.996T>C	XP_005273299.2:p.Phe332=
XM_005273243.3:c.996T>C	XP_005273300.2:p.Phe332=
XM_006711504.2:c.996T>C	XP_006711567.1:p.Phe332=
XM_006711505.2:c.996T>C	XP_006711568.1:p.Phe332=
XM_006711506.2:c.996T>C	XP_006711569.1:p.Phe332=
XM_011509937.1:c.996T>C	XP_011508239.1:p.Phe332=
XM_005273241.4:c.996T>C	XP_005273298.2:p.Phe332=
XM_005273242.4:c.996T>C	XP_005273299.2:p.Phe332=
XM_005273243.4:c.996T>C	XP_005273300.2:p.Phe332=
XM_006711504.3:c.996T>C	XP_006711567.1:p.Phe332=
XM_006711505.3:c.996T>C	XP_006711568.1:p.Phe332=
XM_006711506.3:c.996T>C	XP_006711569.1:p.Phe332=
XM_011509937.2:c.996T>C	XP_011508239.1:p.Phe332=
XM_017002208.1:c.996T>C	XP_016857697.1:p.Phe332=
NM_003268.6:c.996T>C MANE Select	NP_003259.2:p.Phe332=