Canonical Allele Identifier: CA11828008
Gene: TLR1 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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