Canonical Allele Identifier: CA1409861

Gene: TLR5

Linked Data

• dbSNP Id: rs764582120
• ExAC: 1:223285240 TTGGTC / T
• gnomAD v2: 1-223285240-TTGGTC-T
• gnomAD v4: 1-223111898-TTGGTC-T
• MyVariant Identifiers: chr1:g.223285241_223285245del (hg19) ; chr1:g.223111899_223111903del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.223111900_223111904del , CM000663.2:g.223111900_223111904del	GRCh38
NC_000001.10:g.223285242_223285246del , CM000663.1:g.223285242_223285246del	GRCh37
NC_000001.9:g.221351865_221351869del	NCBI36
NG_016244.1:g.36380_36384del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642603.2:c.1129_1133del MANE Select	ENSP00000496355.1:p.Asp377AsnfsTer?
ENST00000645434.1:c.1129_1133del	ENSP00000493892.1:p.Asp377AsnfsTer?
ENST00000366881.5:c.1129_1133del	ENSP00000355846.1:p.Asp377AsnfsTer?
ENST00000540964.5:c.1129_1133del	ENSP00000440643.1:p.Asp377AsnfsTer?
NM_003268.5:c.1129_1133del	NP_003259.2:p.Asp377AsnfsTer?
XM_005273241.3:c.1129_1133del	XP_005273298.2:p.Asp377AsnfsTer?
XM_005273242.3:c.1129_1133del	XP_005273299.2:p.Asp377AsnfsTer?
XM_005273243.3:c.1129_1133del	XP_005273300.2:p.Asp377AsnfsTer?
XM_006711504.2:c.1129_1133del	XP_006711567.1:p.Asp377AsnfsTer?
XM_006711505.2:c.1129_1133del	XP_006711568.1:p.Asp377AsnfsTer?
XM_006711506.2:c.1129_1133del	XP_006711569.1:p.Asp377AsnfsTer?
XM_011509937.1:c.1129_1133del	XP_011508239.1:p.Asp377AsnfsTer?
XM_005273241.4:c.1129_1133del	XP_005273298.2:p.Asp377AsnfsTer?
XM_005273242.4:c.1129_1133del	XP_005273299.2:p.Asp377AsnfsTer?
XM_005273243.4:c.1129_1133del	XP_005273300.2:p.Asp377AsnfsTer?
XM_006711504.3:c.1129_1133del	XP_006711567.1:p.Asp377AsnfsTer?
XM_006711505.3:c.1129_1133del	XP_006711568.1:p.Asp377AsnfsTer?
XM_006711506.3:c.1129_1133del	XP_006711569.1:p.Asp377AsnfsTer?
XM_011509937.2:c.1129_1133del	XP_011508239.1:p.Asp377AsnfsTer?
XM_017002208.1:c.1129_1133del	XP_016857697.1:p.Asp377AsnfsTer?
NM_003268.6:c.1129_1133del MANE Select	NP_003259.2:p.Asp377AsnfsTer?