Canonical Allele Identifier: CA10948689
Gene: TLR5 HGNC NCBI

Linked Data

dbSNP Id: rs5744105
gnomAD v2: 1-223316077-G-C
gnomAD v3: 1-223142735-G-C
gnomAD v4: 1-223142735-G-C
MyVariant Identifiers: chr1:g.223316077G>C (hg19) chr1:g.223142735G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.223142735G>C , CM000663.2:g.223142735G>C GRCh38
NC_000001.10:g.223316077G>C , CM000663.1:g.223316077G>C GRCh37
NC_000001.9:g.221382700G>C NCBI36
NG_016244.1:g.5548C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642603.2:c.-555+461C>G MANE Select ENSP00000496355.1:n.-555+461C>G
ENST00000645434.1:c.-469+461C>G ENSP00000493892.1:n.-469+461C>G
ENST00000646044.1:n.53+461C>G
ENST00000366881.5:c.-555+461C>G ENSP00000355846.1:n.-555+461C>G
ENST00000407096.6:c.-353+461C>G ENSP00000385458.2:n.-353+461C>G
ENST00000465726.1:n.53+461C>G
ENST00000484766.1:n.51+461C>G
NM_003268.5:c.-555+461C>G NP_003259.2:n.-555+461C>G
XM_005273241.3:c.-533+461C>G XP_005273298.2:n.-533+461C>G
XM_005273242.3:c.-649+461C>G XP_005273299.2:n.-649+461C>G
XM_005273243.3:c.-439+461C>G XP_005273300.2:n.-439+461C>G
XM_006711504.2:c.-447+461C>G XP_006711567.1:n.-447+461C>G
XM_006711505.2:c.-353+461C>G XP_006711568.1:n.-353+461C>G
XM_006711506.2:c.-170+461C>G XP_006711569.1:n.-170+461C>G
XM_011509937.1:c.-563+461C>G XP_011508239.1:n.-563+461C>G
XM_005273241.4:c.-533+461C>G XP_005273298.2:n.-533+461C>G
XM_005273242.4:c.-649+461C>G XP_005273299.2:n.-649+461C>G
XM_005273243.4:c.-439+461C>G XP_005273300.2:n.-439+461C>G
XM_006711504.3:c.-447+461C>G XP_006711567.1:n.-447+461C>G
XM_006711505.3:c.-353+461C>G XP_006711568.1:n.-353+461C>G
XM_006711506.3:c.-170+461C>G XP_006711569.1:n.-170+461C>G
XM_011509937.2:c.-563+461C>G XP_011508239.1:n.-563+461C>G
XM_017002208.1:c.-469+461C>G XP_016857697.1:n.-469+461C>G
NM_003268.6:c.-555+461C>G MANE Select NP_003259.2:n.-555+461C>G
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