Canonical Allele Identifier: CA602355439

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126276890del , CM000673.2:g.126276890del	GRCh38
NC_000011.9:g.126146785del , CM000673.1:g.126146785del	GRCh37
NC_000011.8:g.125651995del	NCBI36
NG_028029.1:g.12851del

Transcript Alleles

HGVS	Amino-acid Change
NM_017547.4:c.1102-181del MANE Select	NP_060017.1:n.1102-181del
ENST00000263578.10:c.1102-181del MANE Select	ENSP00000263578.5:n.1102-181del
NM_017547.3:c.1102-181del	NP_060017.1:n.1102-181del
NR_037647.1:n.1048-181del
NR_037647.2:n.934-181del
NR_037648.1:n.1288-181del
NR_037648.2:n.1279-181del
ENST00000263578.9:c.1102-181del	ENSP00000263578.5:n.1102-181del
ENST00000525083.5:n.822-108del
ENST00000525083.6:n.1585-181del
ENST00000525770.5:c.*734-181del	ENSP00000434739.1:n.*734-181del
ENST00000527004.5:c.*446-181del	ENSP00000436374.1:n.*446-181del
ENST00000530642.1:n.2249-181del
ENST00000532101.6:n.1231-181del
ENST00000532125.1:c.1060-181del	ENSP00000434178.1:n.1060-181del
ENST00000532125.2:c.1099-181del	ENSP00000434178.2:n.1099-181del
ENST00000533839.6:c.454-181del	ENSP00000509952.1:n.454-181del
ENST00000534011.5:n.1154-181del
ENST00000534011.6:n.1335-181del
ENST00000534315.5:n.1414-181del
ENST00000685484.1:c.1102-181del	ENSP00000510622.1:n.1102-181del
ENST00000685601.1:c.*154-181del	ENSP00000510603.1:n.*154-181del
ENST00000685765.1:c.*90-181del	ENSP00000509991.1:n.*90-181del
ENST00000685844.1:c.*639-108del	ENSP00000509820.1:n.*639-108del
ENST00000685857.1:n.2206-181del
ENST00000686242.1:c.901-181del	ENSP00000508950.1:n.901-181del
ENST00000686888.1:c.*669-181del	ENSP00000509619.1:n.*669-181del
ENST00000687699.1:c.1226-181del	ENSP00000508878.1:n.1226-181del
ENST00000687786.1:n.2538-181del
ENST00000688100.1:n.1995-181del
ENST00000688588.1:c.972-181del	ENSP00000510802.1:n.972-181del
ENST00000688927.1:n.3313-181del
ENST00000689283.1:c.*765-181del	ENSP00000509050.1:n.*765-181del
ENST00000689477.1:c.*995-181del	ENSP00000508945.1:n.*995-181del
ENST00000689765.1:c.*595-181del	ENSP00000509625.1:n.*595-181del
ENST00000690512.1:c.*953-181del	ENSP00000509793.1:n.*953-181del
ENST00000692039.1:c.*927-181del	ENSP00000508821.1:n.*927-181del
ENST00000692336.1:c.1126-181del	ENSP00000508540.1:n.1126-181del
ENST00000693133.1:n.1947-181del
XM_006718879.2:c.592-181del	XP_006718942.1:n.592-181del
XM_006718879.3:c.592-181del	XP_006718942.1:n.592-181del
XM_006718880.2:c.469-181del	XP_006718943.1:n.469-181del
XM_006718881.2:c.469-181del	XP_006718944.1:n.469-181del
XM_006718881.3:c.469-181del	XP_006718944.1:n.469-181del
XM_011542895.1:c.592-181del	XP_011541197.1:n.592-181del
XM_011542895.2:c.592-181del	XP_011541197.1:n.592-181del
XM_011542896.1:c.592-181del	XP_011541198.1:n.592-181del
XM_011542896.2:c.592-181del	XP_011541198.1:n.592-181del
XM_017018000.2:c.1102-184del	XP_016873489.1:n.1102-184del
XM_017018001.1:c.592-181del	XP_016873490.1:n.592-181del
XM_017018002.1:c.592-181del	XP_016873491.1:n.592-181del
XM_017018003.2:c.469-181del	XP_016873492.1:n.469-181del
XM_017018004.1:c.469-181del	XP_016873493.1:n.469-181del
XM_017018005.1:c.469-181del	XP_016873494.1:n.469-181del
XM_017018006.2:c.469-184del	XP_016873495.1:n.469-184del