Canonical Allele Identifier: CA1451826121

Gene: TLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38798593C= , CM000666.2:g.38798593C=	GRCh38
NC_000004.11:g.38800214C= , CM000666.1:g.38800214C=	GRCh37
NC_000004.10:g.38476609C=	NCBI36
NG_016228.1:g.11199G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003263.4:c.239G= MANE Select	NP_003254.2:p.Arg80=
ENST00000308979.7:c.239G= MANE Select	ENSP00000354932.2:p.Arg80=
NM_003263.3:c.239G=	NP_003254.2:p.Arg80=
ENST00000308979.6:c.239G=	ENSP00000354932.2:p.Arg80=
ENST00000502213.6:c.239G=	ENSP00000421259.1:p.Arg80=
ENST00000505744.5:n.235+2264G=
ENST00000505940.1:c.239G=	ENSP00000421856.1:p.Arg80=
ENST00000515861.5:c.239G=	ENSP00000423017.1:p.Arg80=
XM_005262662.3:c.239G=	XP_005262719.1:p.Arg80=
XM_005262662.5:c.239G=	XP_005262719.1:p.Arg80=
XM_006714028.2:c.239G=	XP_006714091.1:p.Arg80=
XM_011513742.1:c.239G=	XP_011512044.1:p.Arg80=
XM_011513742.3:c.239G=	XP_011512044.1:p.Arg80=
XM_011513743.1:c.239G=	XP_011512045.1:p.Arg80=
XM_011513744.1:c.239G=	XP_011512046.1:p.Arg80=
XM_011513745.1:c.239G=	XP_011512047.1:p.Arg80=
XM_011513745.3:c.239G=	XP_011512047.1:p.Arg80=
XM_017008571.2:c.239G=	XP_016864060.1:p.Arg80=
XM_017008572.2:c.239G=	XP_016864061.1:p.Arg80=
XM_024454196.1:c.239G=	XP_024309964.1:p.Arg80=
XM_024454197.1:c.239G=	XP_024309965.1:p.Arg80=
XM_024454198.1:c.239G=	XP_024309966.1:p.Arg80=
XM_024454199.1:c.205+2264G=	XP_024309967.1:n.205+2264G=
XR_925162.1:n.513G=
XR_925163.1:n.513G=
XR_925163.2:n.513G=
XR_925165.1:n.513G=
XR_925165.2:n.513G=