Canonical Allele Identifier: CA344693990
Gene: TLR5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.223112011G>C , CM000663.2:g.223112011G>C GRCh38
NC_000001.10:g.223285353G>C , CM000663.1:g.223285353G>C GRCh37
NC_000001.9:g.221351976G>C NCBI36
NG_016244.1:g.36272C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642603.2:c.1021C>G MANE Select ENSP00000496355.1:p.Leu341Val
ENST00000645434.1:c.1021C>G ENSP00000493892.1:p.Leu341Val
ENST00000366881.5:c.1021C>G ENSP00000355846.1:p.Leu341Val
ENST00000540964.5:c.1021C>G ENSP00000440643.1:p.Leu341Val
NM_003268.5:c.1021C>G NP_003259.2:p.Leu341Val
XM_005273241.3:c.1021C>G XP_005273298.2:p.Leu341Val
XM_005273242.3:c.1021C>G XP_005273299.2:p.Leu341Val
XM_005273243.3:c.1021C>G XP_005273300.2:p.Leu341Val
XM_006711504.2:c.1021C>G XP_006711567.1:p.Leu341Val
XM_006711505.2:c.1021C>G XP_006711568.1:p.Leu341Val
XM_006711506.2:c.1021C>G XP_006711569.1:p.Leu341Val
XM_011509937.1:c.1021C>G XP_011508239.1:p.Leu341Val
XM_005273241.4:c.1021C>G XP_005273298.2:p.Leu341Val
XM_005273242.4:c.1021C>G XP_005273299.2:p.Leu341Val
XM_005273243.4:c.1021C>G XP_005273300.2:p.Leu341Val
XM_006711504.3:c.1021C>G XP_006711567.1:p.Leu341Val
XM_006711505.3:c.1021C>G XP_006711568.1:p.Leu341Val
XM_006711506.3:c.1021C>G XP_006711569.1:p.Leu341Val
XM_011509937.2:c.1021C>G XP_011508239.1:p.Leu341Val
XM_017002208.1:c.1021C>G XP_016857697.1:p.Leu341Val
NM_003268.6:c.1021C>G MANE Select NP_003259.2:p.Leu341Val