Canonical Allele Identifier: CA1875354804

Gene: TLR4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117713720_117713723delinsACTT , CM000671.2:g.117713720_117713723delinsACTT	GRCh38
NC_000009.11:g.120475998_120476001delinsACTT , CM000671.1:g.120475998_120476001delinsACTT	GRCh37
NC_000009.10:g.119515819_119515822delinsACTT	NCBI36
NG_011475.1:g.14539_14542delinsACTT
NG_011475.2:g.14318_14321delinsACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.93+9155_93+9158delinsACTT	ENSP00000496197.1:n.93+9155_93+9158delinsACTT
ENST00000697624.1:n.200+9155_200+9158delinsACTT
ENST00000697625.1:c.93+9155_93+9158delinsACTT	ENSP00000513362.1:n.93+9155_93+9158delinsACTT
ENST00000697636.1:c.93+9155_93+9158delinsACTT	ENSP00000513366.1:n.93+9155_93+9158delinsACTT
ENST00000697637.1:c.93+9155_93+9158delinsACTT	ENSP00000513367.1:n.93+9155_93+9158delinsACTT
ENST00000697664.1:c.140+4991_140+4994delinsACTT	ENSP00000513389.1:n.140+4991_140+4994delinsACTT
ENST00000697665.1:c.93+9155_93+9158delinsACTT	ENSP00000513390.1:n.93+9155_93+9158delinsACTT
ENST00000697666.1:c.140+4991_140+4994delinsACTT	ENSP00000513391.1:n.140+4991_140+4994delinsACTT
ENST00000355622.8:c.1592_1595delinsACTT MANE Select	ENSP00000363089.5:p.Asn531=
ENST00000394487.5:c.1472_1475delinsACTT	ENSP00000377997.4:p.Asn491=
ENST00000472304.2:c.*1326_*1329delinsACTT	ENSP00000496429.1:n.*1326_*1329delinsACTT
ENST00000642985.1:c.260+4991_260+4994delinsACTT	ENSP00000493686.1:n.260+4991_260+4994delinsACTT
ENST00000646089.1:c.93+9155_93+9158delinsACTT	ENSP00000496197.1:n.93+9155_93+9158delinsACTT
ENST00000665764.1:c.93+9155_93+9158delinsACTT	ENSP00000499745.1:n.93+9155_93+9158delinsACTT
ENST00000355622.6:c.1592_1595delinsACTT	ENSP00000363089.5:p.Asn531=
ENST00000394487.4:c.1472_1475delinsACTT	ENSP00000377997.4:p.Asn491=
ENST00000472304.1:n.1509_1512delinsACTT
NM_003266.3:c.1472_1475delinsACTT	NP_003257.1:p.Asn491=
NM_138554.4:c.1592_1595delinsACTT	NP_612564.1:p.Asn531=
NM_138557.2:c.992_995delinsACTT	NP_612567.1:p.Asn331=
NM_138554.5:c.1592_1595delinsACTT MANE Select	NP_612564.1:p.Asn531=
NM_003266.4:c.1472_1475delinsACTT	NP_003257.1:p.Asn491=
NM_138557.3:c.992_995delinsACTT	NP_612567.1:p.Asn331=