Canonical Allele Identifier: CA1451810426

Gene: TLR1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.38801442A= , CM000666.2:g.38801442A=	GRCh38
NC_000004.11:g.38803063A= , CM000666.1:g.38803063A=	GRCh37
NC_000004.10:g.38479458A=	NCBI36
NG_016228.1:g.8350T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003263.4:c.-159-494T= MANE Select	NP_003254.2:n.-159-494T=
ENST00000308979.7:c.-159-494T= MANE Select	ENSP00000354932.2:n.-159-494T=
NM_003263.3:c.-159-494T=	NP_003254.2:n.-159-494T=
ENST00000308979.6:c.-159-494T=	ENSP00000354932.2:n.-159-494T=
ENST00000502213.6:c.-159-494T=	ENSP00000421259.1:n.-159-494T=
ENST00000505744.5:n.144-494T=
ENST00000505940.1:c.-67-2544T=	ENSP00000421856.1:n.-67-2544T=
ENST00000506146.5:c.-159-494T=	ENSP00000423725.1:n.-159-494T=
ENST00000508364.1:c.-67-2544T=	ENSP00000424894.1:n.-67-2544T=
ENST00000508535.1:n.500-494T=
ENST00000509754.5:n.114-494T=
ENST00000515861.5:c.-67-2544T=	ENSP00000423017.1:n.-67-2544T=
XM_005262662.3:c.-159-494T=	XP_005262719.1:n.-159-494T=
XM_005262662.5:c.-159-494T=	XP_005262719.1:n.-159-494T=
XM_006714028.2:c.-159-494T=	XP_006714091.1:n.-159-494T=
XM_011513742.1:c.-159-494T=	XP_011512044.1:n.-159-494T=
XM_011513742.3:c.-159-494T=	XP_011512044.1:n.-159-494T=
XM_011513743.1:c.-67-2544T=	XP_011512045.1:n.-67-2544T=
XM_011513744.1:c.-67-2544T=	XP_011512046.1:n.-67-2544T=
XM_011513745.1:c.-67-2544T=	XP_011512047.1:n.-67-2544T=
XM_011513745.3:c.-67-2544T=	XP_011512047.1:n.-67-2544T=
XM_017008571.2:c.-159-494T=	XP_016864060.1:n.-159-494T=
XM_017008572.2:c.-67-2544T=	XP_016864061.1:n.-67-2544T=
XM_024454196.1:c.-159-494T=	XP_024309964.1:n.-159-494T=
XM_024454197.1:c.-67-2544T=	XP_024309965.1:n.-67-2544T=
XM_024454198.1:c.-67-2544T=	XP_024309966.1:n.-67-2544T=
XM_024454199.1:c.114-494T=	XP_024309967.1:n.114-494T=
XR_925162.1:n.116-494T=
XR_925163.1:n.116-494T=
XR_925163.2:n.116-494T=
XR_925165.1:n.116-494T=
XR_925165.2:n.116-494T=