Canonical Allele Identifier: CA1451824634

Gene: TLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38798016_38798019delinsAGTT , CM000666.2:g.38798016_38798019delinsAGTT	GRCh38
NC_000004.11:g.38799637_38799640delinsAGTT , CM000666.1:g.38799637_38799640delinsAGTT	GRCh37
NC_000004.10:g.38476032_38476035delinsAGTT	NCBI36
NG_016228.1:g.11773_11776delinsAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308979.7:c.813_816delinsAACT MANE Select	ENSP00000354932.2:p.Thr271=
ENST00000308979.6:c.813_816delinsAACT	ENSP00000354932.2:p.Thr271=
ENST00000502213.6:c.813_816delinsAACT	ENSP00000421259.1:p.Thr271=
ENST00000505744.5:n.235+2838_235+2841delinsAACT
NM_003263.3:c.813_816delinsAACT	NP_003254.2:p.Thr271=
XM_005262662.3:c.813_816delinsAACT	XP_005262719.1:p.Thr271=
XM_006714028.2:c.813_816delinsAACT	XP_006714091.1:p.Thr271=
XM_011513742.1:c.813_816delinsAACT	XP_011512044.1:p.Thr271=
XM_011513743.1:c.813_816delinsAACT	XP_011512045.1:p.Thr271=
XM_011513744.1:c.813_816delinsAACT	XP_011512046.1:p.Thr271=
XM_011513745.1:c.813_816delinsAACT	XP_011512047.1:p.Thr271=
XR_925162.1:n.1087_1090delinsAACT
XR_925163.1:n.1087_1090delinsAACT
XR_925165.1:n.1087_1090delinsAACT
XM_005262662.5:c.813_816delinsAACT	XP_005262719.1:p.Thr271=
XM_011513742.3:c.813_816delinsAACT	XP_011512044.1:p.Thr271=
XM_011513745.3:c.813_816delinsAACT	XP_011512047.1:p.Thr271=
XM_017008571.2:c.813_816delinsAACT	XP_016864060.1:p.Thr271=
XM_017008572.2:c.813_816delinsAACT	XP_016864061.1:p.Thr271=
XM_024454196.1:c.813_816delinsAACT	XP_024309964.1:p.Thr271=
XM_024454197.1:c.813_816delinsAACT	XP_024309965.1:p.Thr271=
XM_024454198.1:c.813_816delinsAACT	XP_024309966.1:p.Thr271=
XM_024454199.1:c.205+2838_205+2841delinsAACT	XP_024309967.1:n.205+2838_205+2841delinsAACT
XR_925163.2:n.1087_1090delinsAACT
XR_925165.2:n.1087_1090delinsAACT
NM_003263.4:c.813_816delinsAACT MANE Select	NP_003254.2:p.Thr271=