Canonical Allele Identifier: CA423724639

Gene: TLR5

Linked Data

• MyVariant Identifiers: chr1:g.223285201G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.223111859G>T , CM000663.2:g.223111859G>T	GRCh38
NC_000001.10:g.223285201G>T , CM000663.1:g.223285201G>T	GRCh37
NC_000001.9:g.221351824G>T	NCBI36
NG_016244.1:g.36424C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000642603.2:c.1173C>A MANE Select	ENSP00000496355.1:p.Leu391=
ENST00000645434.1:c.1173C>A	ENSP00000493892.1:p.Leu391=
ENST00000366881.5:c.1173C>A	ENSP00000355846.1:p.Leu391=
ENST00000540964.5:c.1173C>A	ENSP00000440643.1:p.Leu391=
NM_003268.5:c.1173C>A	NP_003259.2:p.Leu391=
XM_005273241.3:c.1173C>A	XP_005273298.2:p.Leu391=
XM_005273242.3:c.1173C>A	XP_005273299.2:p.Leu391=
XM_005273243.3:c.1173C>A	XP_005273300.2:p.Leu391=
XM_006711504.2:c.1173C>A	XP_006711567.1:p.Leu391=
XM_006711505.2:c.1173C>A	XP_006711568.1:p.Leu391=
XM_006711506.2:c.1173C>A	XP_006711569.1:p.Leu391=
XM_011509937.1:c.1173C>A	XP_011508239.1:p.Leu391=
XM_005273241.4:c.1173C>A	XP_005273298.2:p.Leu391=
XM_005273242.4:c.1173C>A	XP_005273299.2:p.Leu391=
XM_005273243.4:c.1173C>A	XP_005273300.2:p.Leu391=
XM_006711504.3:c.1173C>A	XP_006711567.1:p.Leu391=
XM_006711505.3:c.1173C>A	XP_006711568.1:p.Leu391=
XM_006711506.3:c.1173C>A	XP_006711569.1:p.Leu391=
XM_011509937.2:c.1173C>A	XP_011508239.1:p.Leu391=
XM_017002208.1:c.1173C>A	XP_016857697.1:p.Leu391=
NM_003268.6:c.1173C>A MANE Select	NP_003259.2:p.Leu391=