Canonical Allele Identifier: CA11685797
Gene: TLR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38804362T>C , CM000666.2:g.38804362T>C GRCh38
NC_000004.11:g.38805983T>C , CM000666.1:g.38805983T>C GRCh37
NC_000004.10:g.38482378T>C NCBI36
NG_016228.1:g.5430A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308979.7:c.-216A>G MANE Select ENSP00000354932.2:n.-216A>G
ENST00000308979.6:c.-216A>G ENSP00000354932.2:n.-216A>G
ENST00000502213.6:c.-216A>G ENSP00000421259.1:n.-216A>G
ENST00000505744.5:n.87A>G
ENST00000505940.1:c.-68+392A>G ENSP00000421856.1:n.-68+392A>G
ENST00000506146.5:c.-216A>G ENSP00000423725.1:n.-216A>G
ENST00000508364.1:c.-68+750A>G ENSP00000424894.1:n.-68+750A>G
ENST00000508535.1:n.443A>G
ENST00000509754.5:n.57A>G
ENST00000515861.5:c.-124A>G ENSP00000423017.1:n.-124A>G
NM_003263.3:c.-216A>G NP_003254.2:n.-216A>G
XM_005262662.3:c.-216A>G XP_005262719.1:n.-216A>G
XM_011513742.1:c.-160+392A>G XP_011512044.1:n.-160+392A>G
XM_011513743.1:c.-124A>G XP_011512045.1:n.-124A>G
XM_011513744.1:c.-68+392A>G XP_011512046.1:n.-68+392A>G
XM_011513745.1:c.-68+392A>G XP_011512047.1:n.-68+392A>G
XR_925162.1:n.59A>G
XR_925163.1:n.59A>G
XR_925165.1:n.59A>G
XM_005262662.5:c.-216A>G XP_005262719.1:n.-216A>G
XM_011513742.3:c.-160+392A>G XP_011512044.1:n.-160+392A>G
XM_011513745.3:c.-68+392A>G XP_011512047.1:n.-68+392A>G
XM_017008571.2:c.-216A>G XP_016864060.1:n.-216A>G
XM_017008572.2:c.-124A>G XP_016864061.1:n.-124A>G
XM_024454196.1:c.-160+392A>G XP_024309964.1:n.-160+392A>G
XM_024454197.1:c.-124A>G XP_024309965.1:n.-124A>G
XM_024454198.1:c.-68+392A>G XP_024309966.1:n.-68+392A>G
XM_024454199.1:c.113+392A>G XP_024309967.1:n.113+392A>G
XR_925163.2:n.59A>G
XR_925165.2:n.59A>G
NM_003263.4:c.-216A>G MANE Select NP_003254.2:n.-216A>G
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