Canonical Allele Identifier: CA1223521569

Gene: TLR5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.223112014_223112021delinsCTTGGAGG , CM000663.2:g.223112014_223112021delinsCTTGGAGG	GRCh38
NC_000001.10:g.223285356_223285363delinsCTTGGAGG , CM000663.1:g.223285356_223285363delinsCTTGGAGG	GRCh37
NC_000001.9:g.221351979_221351986delinsCTTGGAGG	NCBI36
NG_016244.1:g.36262_36269delinsCCTCCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642603.2:c.1011_1018delinsCCTCCAAG MANE Select	ENSP00000496355.1:p.Asn337=
ENST00000645434.1:c.1011_1018delinsCCTCCAAG	ENSP00000493892.1:p.Asn337=
ENST00000366881.5:c.1011_1018delinsCCTCCAAG	ENSP00000355846.1:p.Asn337=
ENST00000540964.5:c.1011_1018delinsCCTCCAAG	ENSP00000440643.1:p.Asn337=
NM_003268.5:c.1011_1018delinsCCTCCAAG	NP_003259.2:p.Asn337=
XM_005273241.3:c.1011_1018delinsCCTCCAAG	XP_005273298.2:p.Asn337=
XM_005273242.3:c.1011_1018delinsCCTCCAAG	XP_005273299.2:p.Asn337=
XM_005273243.3:c.1011_1018delinsCCTCCAAG	XP_005273300.2:p.Asn337=
XM_006711504.2:c.1011_1018delinsCCTCCAAG	XP_006711567.1:p.Asn337=
XM_006711505.2:c.1011_1018delinsCCTCCAAG	XP_006711568.1:p.Asn337=
XM_006711506.2:c.1011_1018delinsCCTCCAAG	XP_006711569.1:p.Asn337=
XM_011509937.1:c.1011_1018delinsCCTCCAAG	XP_011508239.1:p.Asn337=
XM_005273241.4:c.1011_1018delinsCCTCCAAG	XP_005273298.2:p.Asn337=
XM_005273242.4:c.1011_1018delinsCCTCCAAG	XP_005273299.2:p.Asn337=
XM_005273243.4:c.1011_1018delinsCCTCCAAG	XP_005273300.2:p.Asn337=
XM_006711504.3:c.1011_1018delinsCCTCCAAG	XP_006711567.1:p.Asn337=
XM_006711505.3:c.1011_1018delinsCCTCCAAG	XP_006711568.1:p.Asn337=
XM_006711506.3:c.1011_1018delinsCCTCCAAG	XP_006711569.1:p.Asn337=
XM_011509937.2:c.1011_1018delinsCCTCCAAG	XP_011508239.1:p.Asn337=
XM_017002208.1:c.1011_1018delinsCCTCCAAG	XP_016857697.1:p.Asn337=
NM_003268.6:c.1011_1018delinsCCTCCAAG MANE Select	NP_003259.2:p.Asn337=