Canonical Allele Identifier: CA2616722454

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275365-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275366del , CM000673.2:g.126275366del	GRCh38
NC_000011.9:g.126145261del , CM000673.1:g.126145261del	GRCh37
NC_000011.8:g.125650471del	NCBI36
NG_028029.1:g.11327del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1154del
ENST00000532101.6:n.773del
ENST00000532125.2:c.668del	ENSP00000434178.2:p.Leu223ProfsTer20
ENST00000533839.6:c.86-428del	ENSP00000509952.1:n.86-428del
ENST00000534011.6:n.963del
ENST00000685484.1:c.671del	ENSP00000510622.1:p.Leu224ProfsTer20
ENST00000685601.1:c.671del	ENSP00000510603.1:p.Leu224ProfsTer20
ENST00000685765.1:c.671del	ENSP00000509991.1:p.Leu224ProfsTer20
ENST00000685844.1:c.*208del	ENSP00000509820.1:n.*208del
ENST00000685857.1:n.1410del
ENST00000686242.1:c.470del	ENSP00000508950.1:n.470del
ENST00000686888.1:c.*238del	ENSP00000509619.1:n.*238del
ENST00000687699.1:c.795del	ENSP00000508878.1:n.795del
ENST00000687786.1:n.2107del
ENST00000688100.1:n.1592del
ENST00000688588.1:c.671del	ENSP00000510802.1:p.Leu224ProfsTer20
ENST00000688927.1:n.2882del
ENST00000689283.1:c.*334del	ENSP00000509050.1:n.*334del
ENST00000689477.1:c.*564del	ENSP00000508945.1:n.*564del
ENST00000689765.1:c.*169-5del	ENSP00000509625.1:n.*169-5del
ENST00000690512.1:c.*522del	ENSP00000509793.1:n.*522del
ENST00000692039.1:c.*469del	ENSP00000508821.1:n.*469del
ENST00000692336.1:c.695del	ENSP00000508540.1:p.Leu232ProfsTer20
ENST00000693133.1:n.1151del
ENST00000263578.10:c.671del MANE Select	ENSP00000263578.5:p.Leu224ProfsTer20
ENST00000263578.9:c.671del	ENSP00000263578.5:p.Leu224ProfsTer20
ENST00000525083.5:n.391del
ENST00000525770.5:c.*303del	ENSP00000434739.1:n.*303del
ENST00000527004.5:c.*15del	ENSP00000436374.1:n.*15del
ENST00000530642.1:n.1453del
ENST00000532101.5:n.894del
ENST00000532125.1:c.629del	ENSP00000434178.1:p.Leu210ProfsTer20
ENST00000533395.5:n.404del
ENST00000533839.5:n.238-428del
ENST00000534011.5:n.723del
ENST00000534315.5:n.983del
NM_017547.3:c.671del	NP_060017.1:p.Leu224ProfsTer20
NR_037647.1:n.617del
NR_037648.1:n.857del
XM_006718879.2:c.161del	XP_006718942.1:p.Leu54ProfsTer20
XM_006718880.2:c.38del	XP_006718943.1:p.Leu13ProfsTer20
XM_006718881.2:c.38del	XP_006718944.1:p.Leu13ProfsTer20
XM_011542895.1:c.161del	XP_011541197.1:p.Leu54ProfsTer20
XM_011542896.1:c.161del	XP_011541198.1:p.Leu54ProfsTer20
XM_006718879.3:c.161del	XP_006718942.1:p.Leu54ProfsTer20
XM_006718881.3:c.38del	XP_006718944.1:p.Leu13ProfsTer20
XM_011542895.2:c.161del	XP_011541197.1:p.Leu54ProfsTer20
XM_011542896.2:c.161del	XP_011541198.1:p.Leu54ProfsTer20
XM_017018000.2:c.671del	XP_016873489.1:p.Leu224ProfsTer20
XM_017018001.1:c.161del	XP_016873490.1:p.Leu54ProfsTer20
XM_017018002.1:c.161del	XP_016873491.1:p.Leu54ProfsTer20
XM_017018003.2:c.38del	XP_016873492.1:p.Leu13ProfsTer20
XM_017018004.1:c.38del	XP_016873493.1:p.Leu13ProfsTer20
XM_017018005.1:c.38del	XP_016873494.1:p.Leu13ProfsTer20
XM_017018006.2:c.38del	XP_016873495.1:p.Leu13ProfsTer20
NM_017547.4:c.671del MANE Select	NP_060017.1:p.Leu224ProfsTer20
NR_037647.2:n.503del
NR_037648.2:n.848del