Canonical Allele Identifier: CA2616722453

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275362-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275363_126275364del , CM000673.2:g.126275363_126275364del	GRCh38
NC_000011.9:g.126145258_126145259del , CM000673.1:g.126145258_126145259del	GRCh37
NC_000011.8:g.125650468_125650469del	NCBI36
NG_028029.1:g.11324_11325del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1151_1152del
ENST00000532101.6:n.770_771del
ENST00000532125.2:c.665_666del	ENSP00000434178.2:p.Leu222ProfsTer?
ENST00000533839.6:c.86-431_86-430del	ENSP00000509952.1:n.86-431_86-430del
ENST00000534011.6:n.960_961del
ENST00000685484.1:c.668_669del	ENSP00000510622.1:p.Leu223ProfsTer?
ENST00000685601.1:c.668_669del	ENSP00000510603.1:p.Leu223ProfsTer?
ENST00000685765.1:c.668_669del	ENSP00000509991.1:p.Leu223ProfsTer?
ENST00000685844.1:c.*205_*206del	ENSP00000509820.1:n.*205_*206del
ENST00000685857.1:n.1407_1408del
ENST00000686242.1:c.467_468del	ENSP00000508950.1:n.467_468del
ENST00000686888.1:c.*235_*236del	ENSP00000509619.1:n.*235_*236del
ENST00000687699.1:c.792_793del	ENSP00000508878.1:n.792_793del
ENST00000687786.1:n.2104_2105del
ENST00000688100.1:n.1589_1590del
ENST00000688588.1:c.668_669del	ENSP00000510802.1:p.Leu223ProfsTer?
ENST00000688927.1:n.2879_2880del
ENST00000689283.1:c.*331_*332del	ENSP00000509050.1:n.*331_*332del
ENST00000689477.1:c.*561_*562del	ENSP00000508945.1:n.*561_*562del
ENST00000689765.1:c.*169-8_*169-7del	ENSP00000509625.1:n.*169-8_*169-7del
ENST00000690512.1:c.*519_*520del	ENSP00000509793.1:n.*519_*520del
ENST00000692039.1:c.*466_*467del	ENSP00000508821.1:n.*466_*467del
ENST00000692336.1:c.692_693del	ENSP00000508540.1:p.Leu231ProfsTer?
ENST00000693133.1:n.1148_1149del
ENST00000263578.10:c.668_669del MANE Select	ENSP00000263578.5:p.Leu223ProfsTer?
ENST00000263578.9:c.668_669del	ENSP00000263578.5:p.Leu223ProfsTer?
ENST00000525083.5:n.388_389del
ENST00000525770.5:c.*300_*301del	ENSP00000434739.1:n.*300_*301del
ENST00000527004.5:c.*12_*13del	ENSP00000436374.1:n.*12_*13del
ENST00000530642.1:n.1450_1451del
ENST00000532101.5:n.891_892del
ENST00000532125.1:c.626_627del	ENSP00000434178.1:p.Leu209ProfsTer?
ENST00000533395.5:n.401_402del
ENST00000533839.5:n.238-431_238-430del
ENST00000534011.5:n.720_721del
ENST00000534315.5:n.980_981del
NM_017547.3:c.668_669del	NP_060017.1:p.Leu223ProfsTer?
NR_037647.1:n.614_615del
NR_037648.1:n.854_855del
XM_006718879.2:c.158_159del	XP_006718942.1:p.Leu53ProfsTer?
XM_006718880.2:c.35_36del	XP_006718943.1:p.Leu12ProfsTer?
XM_006718881.2:c.35_36del	XP_006718944.1:p.Leu12ProfsTer?
XM_011542895.1:c.158_159del	XP_011541197.1:p.Leu53ProfsTer?
XM_011542896.1:c.158_159del	XP_011541198.1:p.Leu53ProfsTer?
XM_006718879.3:c.158_159del	XP_006718942.1:p.Leu53ProfsTer?
XM_006718881.3:c.35_36del	XP_006718944.1:p.Leu12ProfsTer?
XM_011542895.2:c.158_159del	XP_011541197.1:p.Leu53ProfsTer?
XM_011542896.2:c.158_159del	XP_011541198.1:p.Leu53ProfsTer?
XM_017018000.2:c.668_669del	XP_016873489.1:p.Leu223ProfsTer?
XM_017018001.1:c.158_159del	XP_016873490.1:p.Leu53ProfsTer?
XM_017018002.1:c.158_159del	XP_016873491.1:p.Leu53ProfsTer?
XM_017018003.2:c.35_36del	XP_016873492.1:p.Leu12ProfsTer?
XM_017018004.1:c.35_36del	XP_016873493.1:p.Leu12ProfsTer?
XM_017018005.1:c.35_36del	XP_016873494.1:p.Leu12ProfsTer?
XM_017018006.2:c.35_36del	XP_016873495.1:p.Leu12ProfsTer?
NM_017547.4:c.668_669del MANE Select	NP_060017.1:p.Leu223ProfsTer?
NR_037647.2:n.500_501del
NR_037648.2:n.845_846del