Canonical Allele Identifier: CA2616719079
Gene: FOXRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126271607_126271622dup , CM000673.2:g.126271607_126271622dup GRCh38
NC_000011.9:g.126141502_126141517dup , CM000673.1:g.126141502_126141517dup GRCh37
NC_000011.8:g.125646712_125646727dup NCBI36
NG_028029.1:g.7568_7583dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.434_449dup
ENST00000532101.6:n.433_448dup
ENST00000532125.2:c.256_271dup ENSP00000434178.2:p.Ala91GlyfsTer?
ENST00000533839.6:c.85+2316_85+2331dup ENSP00000509952.1:n.85+2316_85+2331dup
ENST00000534011.6:n.532_547dup
ENST00000685484.1:c.256_271dup ENSP00000510622.1:p.Ala91GlyfsTer?
ENST00000685601.1:c.256_271dup ENSP00000510603.1:p.Ala91GlyfsTer?
ENST00000685765.1:c.256_271dup ENSP00000509991.1:p.Ala91GlyfsTer?
ENST00000685844.1:c.86-1362_86-1347dup ENSP00000509820.1:n.86-1362_86-1347dup
ENST00000685857.1:n.434_449dup
ENST00000686242.1:c.86-1362_86-1347dup ENSP00000508950.1:n.86-1362_86-1347dup
ENST00000686888.1:c.256_271dup ENSP00000509619.1:p.Ala91GlyfsTer?
ENST00000687699.1:c.380_395dup ENSP00000508878.1:n.380_395dup
ENST00000687786.1:n.1589_1604dup
ENST00000688588.1:c.256_271dup ENSP00000510802.1:p.Ala91GlyfsTer?
ENST00000688927.1:n.434_449dup
ENST00000689283.1:c.210-1362_210-1347dup ENSP00000509050.1:n.210-1362_210-1347dup
ENST00000689477.1:c.*149_*164dup ENSP00000508945.1:n.*149_*164dup
ENST00000689765.1:c.86-1362_86-1347dup ENSP00000509625.1:n.86-1362_86-1347dup
ENST00000690512.1:c.86-871_86-856dup ENSP00000509793.1:n.86-871_86-856dup
ENST00000692039.1:c.*54_*69dup ENSP00000508821.1:n.*54_*69dup
ENST00000692336.1:c.256_271dup ENSP00000508540.1:p.Ala91GlyfsTer?
ENST00000693133.1:n.226-1362_226-1347dup
ENST00000263578.10:c.256_271dup MANE Select ENSP00000263578.5:p.Ala91GlyfsTer?
ENST00000263578.9:c.256_271dup ENSP00000263578.5:p.Ala91GlyfsTer?
ENST00000524751.5:n.223-1362_223-1347dup
ENST00000525083.5:n.122-1362_122-1347dup
ENST00000525770.5:c.86-1362_86-1347dup ENSP00000434739.1:n.86-1362_86-1347dup
ENST00000526366.5:n.101-112_101-97dup
ENST00000526525.1:n.246-1362_246-1347dup
ENST00000527004.5:c.256_271dup ENSP00000436374.1:p.Ala91GlyfsTer?
ENST00000529802.1:n.306_321dup
ENST00000532101.5:n.479_494dup
ENST00000532125.1:c.214_229dup ENSP00000434178.1:p.Ala77GlyfsTer?
ENST00000533839.5:n.237+2316_237+2331dup
ENST00000534011.5:n.158-871_158-856dup
ENST00000534315.5:n.663_678dup
NM_017547.3:c.256_271dup NP_060017.1:p.Ala91GlyfsTer?
NR_037647.1:n.253-1362_253-1347dup
NR_037648.1:n.442_457dup
XM_006718880.2:c.-283_-268dup XP_006718943.1:n.-283_-268dup
XM_006718881.2:c.-232-1362_-232-1347dup XP_006718944.1:n.-232-1362_-232-1347dup
XM_011542895.1:c.-255_-240dup XP_011541197.1:n.-255_-240dup
XM_011542896.1:c.-275_-260dup XP_011541198.1:n.-275_-260dup
XM_006718881.3:c.-232-1362_-232-1347dup XP_006718944.1:n.-232-1362_-232-1347dup
XM_011542895.2:c.-255_-240dup XP_011541197.1:n.-255_-240dup
XM_011542896.2:c.-275_-260dup XP_011541198.1:n.-275_-260dup
XM_017018000.2:c.256_271dup XP_016873489.1:p.Ala91GlyfsTer?
XM_017018001.1:c.-275_-260dup XP_016873490.1:n.-275_-260dup
XM_017018002.1:c.-224-1362_-224-1347dup XP_016873491.1:n.-224-1362_-224-1347dup
XM_017018003.2:c.-283_-268dup XP_016873492.1:n.-283_-268dup
XM_017018004.1:c.-283_-268dup XP_016873493.1:n.-283_-268dup
XM_017018005.1:c.-481_-466dup XP_016873494.1:n.-481_-466dup
XM_017018006.2:c.-283_-268dup XP_016873495.1:n.-283_-268dup
NM_017547.4:c.256_271dup MANE Select NP_060017.1:p.Ala91GlyfsTer?
NR_037647.2:n.139-1362_139-1347dup
NR_037648.2:n.433_448dup