Canonical Allele Identifier: CA2569587600

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271183_126271187del , CM000673.2:g.126271183_126271187del	GRCh38
NC_000011.9:g.126141078_126141082del , CM000673.1:g.126141078_126141082del	GRCh37
NC_000011.8:g.125646288_125646292del	NCBI36
NG_028029.1:g.7144_7148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-254_264-250del
ENST00000532101.6:n.46-37_46-33del
ENST00000532125.2:c.86-254_86-250del	ENSP00000434178.2:n.86-254_86-250del
ENST00000533839.6:c.85+1892_85+1896del	ENSP00000509952.1:n.85+1892_85+1896del
ENST00000534011.6:n.145-37_145-33del
ENST00000685484.1:c.86-254_86-250del	ENSP00000510622.1:n.86-254_86-250del
ENST00000685601.1:c.86-254_86-250del	ENSP00000510603.1:n.86-254_86-250del
ENST00000685765.1:c.86-254_86-250del	ENSP00000509991.1:n.86-254_86-250del
ENST00000685844.1:c.86-1786_86-1782del	ENSP00000509820.1:n.86-1786_86-1782del
ENST00000685857.1:n.264-254_264-250del
ENST00000686242.1:c.86-1786_86-1782del	ENSP00000508950.1:n.86-1786_86-1782del
ENST00000686888.1:c.86-254_86-250del	ENSP00000509619.1:n.86-254_86-250del
ENST00000687699.1:c.210-254_210-250del	ENSP00000508878.1:n.210-254_210-250del
ENST00000687786.1:n.1165_1169del
ENST00000688588.1:c.86-254_86-250del	ENSP00000510802.1:n.86-254_86-250del
ENST00000688927.1:n.264-254_264-250del
ENST00000689283.1:c.209+1768_209+1772del	ENSP00000509050.1:n.209+1768_209+1772del
ENST00000689477.1:c.86-37_86-33del	ENSP00000508945.1:n.86-37_86-33del
ENST00000689765.1:c.86-1786_86-1782del	ENSP00000509625.1:n.86-1786_86-1782del
ENST00000690512.1:c.86-1295_86-1291del	ENSP00000509793.1:n.86-1295_86-1291del
ENST00000692039.1:c.86-168_86-164del	ENSP00000508821.1:n.86-168_86-164del
ENST00000692336.1:c.86-254_86-250del	ENSP00000508540.1:n.86-254_86-250del
ENST00000693133.1:n.225+1768_225+1772del
ENST00000263578.10:c.86-254_86-250del MANE Select	ENSP00000263578.5:n.86-254_86-250del
ENST00000263578.9:c.86-254_86-250del	ENSP00000263578.5:n.86-254_86-250del
ENST00000524751.5:n.222+1768_222+1772del
ENST00000525083.5:n.122-1786_122-1782del
ENST00000525770.5:c.86-1786_86-1782del	ENSP00000434739.1:n.86-1786_86-1782del
ENST00000526366.5:n.101-536_101-532del
ENST00000526525.1:n.245+1768_245+1772del
ENST00000527004.5:c.86-254_86-250del	ENSP00000436374.1:n.86-254_86-250del
ENST00000529802.1:n.136-254_136-250del
ENST00000532101.5:n.92-37_92-33del
ENST00000532125.1:c.44-254_44-250del	ENSP00000434178.1:n.44-254_44-250del
ENST00000533839.5:n.237+1892_237+1896del
ENST00000534011.5:n.158-1295_158-1291del
ENST00000534315.5:n.239_243del
NM_017547.3:c.86-254_86-250del	NP_060017.1:n.86-254_86-250del
NR_037647.1:n.253-1786_253-1782del
NR_037648.1:n.272-254_272-250del
XM_006718880.2:c.-707_-703del	XP_006718943.1:n.-707_-703del
XM_006718881.2:c.-232-1786_-232-1782del	XP_006718944.1:n.-232-1786_-232-1782del
XM_011542895.1:c.-642-37_-642-33del	XP_011541197.1:n.-642-37_-642-33del
XM_011542896.1:c.-445-254_-445-250del	XP_011541198.1:n.-445-254_-445-250del
XM_006718881.3:c.-232-1786_-232-1782del	XP_006718944.1:n.-232-1786_-232-1782del
XM_011542895.2:c.-642-37_-642-33del	XP_011541197.1:n.-642-37_-642-33del
XM_011542896.2:c.-445-254_-445-250del	XP_011541198.1:n.-445-254_-445-250del
XM_017018000.2:c.86-254_86-250del	XP_016873489.1:n.86-254_86-250del
XM_017018001.1:c.-445-254_-445-250del	XP_016873490.1:n.-445-254_-445-250del
XM_017018002.1:c.-224-1786_-224-1782del	XP_016873491.1:n.-224-1786_-224-1782del
XM_017018003.2:c.-453-254_-453-250del	XP_016873492.1:n.-453-254_-453-250del
XM_017018004.1:c.-670-37_-670-33del	XP_016873493.1:n.-670-37_-670-33del
XM_017018005.1:c.-905_-901del	XP_016873494.1:n.-905_-901del
XM_017018006.2:c.-453-254_-453-250del	XP_016873495.1:n.-453-254_-453-250del
NM_017547.4:c.86-254_86-250del MANE Select	NP_060017.1:n.86-254_86-250del
NR_037647.2:n.139-1786_139-1782del
NR_037648.2:n.263-254_263-250del