Canonical Allele Identifier: CA2007079537
Gene: FOXRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126274960T= , CM000673.2:g.126274960T= GRCh38
NC_000011.9:g.126144855T= , CM000673.1:g.126144855T= GRCh37
NC_000011.8:g.125650065T= NCBI36
NG_028029.1:g.10921T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.748T=
ENST00000532101.6:n.734-367T=
ENST00000532125.2:c.567T= ENSP00000434178.2:p.Pro189=
ENST00000533839.6:c.86-834T= ENSP00000509952.1:n.86-834T=
ENST00000534011.6:n.862T=
ENST00000685484.1:c.570T= ENSP00000510622.1:p.Pro190=
ENST00000685601.1:c.570T= ENSP00000510603.1:p.Pro190=
ENST00000685765.1:c.570T= ENSP00000509991.1:p.Pro190=
ENST00000685844.1:c.*169-367T= ENSP00000509820.1:n.*169-367T=
ENST00000685857.1:n.1004T=
ENST00000686242.1:c.369T= ENSP00000508950.1:n.369T=
ENST00000686888.1:c.*137T= ENSP00000509619.1:n.*137T=
ENST00000687699.1:c.694T= ENSP00000508878.1:n.694T=
ENST00000687786.1:n.2068-367T=
ENST00000688100.1:n.1491T=
ENST00000688588.1:c.570T= ENSP00000510802.1:p.Pro190=
ENST00000688927.1:n.2476T=
ENST00000689283.1:c.*233T= ENSP00000509050.1:n.*233T=
ENST00000689477.1:c.*463T= ENSP00000508945.1:n.*463T=
ENST00000689765.1:c.*169-411T= ENSP00000509625.1:n.*169-411T=
ENST00000690512.1:c.*421T= ENSP00000509793.1:n.*421T=
ENST00000692039.1:c.*368T= ENSP00000508821.1:n.*368T=
ENST00000692336.1:c.594T= ENSP00000508540.1:p.Pro198=
ENST00000693133.1:n.745T=
ENST00000263578.10:c.570T= MANE Select ENSP00000263578.5:p.Pro190=
ENST00000263578.9:c.570T= ENSP00000263578.5:p.Pro190=
ENST00000524751.5:n.506T=
ENST00000525083.5:n.352-367T=
ENST00000525770.5:c.*202T= ENSP00000434739.1:n.*202T=
ENST00000526366.5:n.501T=
ENST00000527004.5:c.534-367T= ENSP00000436374.1:n.534-367T=
ENST00000527875.1:n.400T=
ENST00000530642.1:n.1047T=
ENST00000532101.5:n.793T=
ENST00000532125.1:c.528T= ENSP00000434178.1:p.Pro176=
ENST00000533395.5:n.365-367T=
ENST00000533839.5:n.238-834T=
ENST00000534011.5:n.622T=
ENST00000534315.5:n.944-367T=
NM_017547.3:c.570T= NP_060017.1:p.Pro190=
NR_037647.1:n.516T=
NR_037648.1:n.756T=
XM_006718879.2:c.60T= XP_006718942.1:p.Pro20=
XM_006718880.2:c.-2-367T= XP_006718943.1:n.-2-367T=
XM_006718881.2:c.-2-367T= XP_006718944.1:n.-2-367T=
XM_011542895.1:c.60T= XP_011541197.1:p.Pro20=
XM_011542896.1:c.60T= XP_011541198.1:p.Pro20=
XM_006718879.3:c.60T= XP_006718942.1:p.Pro20=
XM_006718881.3:c.-2-367T= XP_006718944.1:n.-2-367T=
XM_011542895.2:c.60T= XP_011541197.1:p.Pro20=
XM_011542896.2:c.60T= XP_011541198.1:p.Pro20=
XM_017018000.2:c.570T= XP_016873489.1:p.Pro190=
XM_017018001.1:c.60T= XP_016873490.1:p.Pro20=
XM_017018002.1:c.60T= XP_016873491.1:p.Pro20=
XM_017018003.2:c.-2-367T= XP_016873492.1:n.-2-367T=
XM_017018004.1:c.-2-367T= XP_016873493.1:n.-2-367T=
XM_017018005.1:c.-2-367T= XP_016873494.1:n.-2-367T=
XM_017018006.2:c.-2-367T= XP_016873495.1:n.-2-367T=
NM_017547.4:c.570T= MANE Select NP_060017.1:p.Pro190=
NR_037647.2:n.402T=
NR_037648.2:n.747T=