Canonical Allele Identifier: CA673003820

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1477724880
• gnomAD v4: 11-126275393-CCTTGGGAGT-C
• MyVariant Identifiers: chr11:g.126145289_126145297del (hg19) ; chr11:g.126275394_126275402del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275395_126275403del , CM000673.2:g.126275395_126275403del	GRCh38
NC_000011.9:g.126145290_126145298del , CM000673.1:g.126145290_126145298del	GRCh37
NC_000011.8:g.125650500_125650508del	NCBI36
NG_028029.1:g.11356_11364del

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1183_1191del
ENST00000532101.6:n.802_810del
ENST00000532125.2:c.697_705del	ENSP00000434178.2:p.Leu233_Val235del
ENST00000533839.6:c.86-399_86-391del	ENSP00000509952.1:n.86-399_86-391del
ENST00000534011.6:n.992_1000del
ENST00000685484.1:c.700_708del	ENSP00000510622.1:p.Leu234_Val236del
ENST00000685601.1:c.700_708del	ENSP00000510603.1:p.Leu234_Val236del
ENST00000685765.1:c.700_708del	ENSP00000509991.1:p.Leu234_Val236del
ENST00000685844.1:c.*237_*245del	ENSP00000509820.1:n.*237_*245del
ENST00000685857.1:n.1439_1447del
ENST00000686242.1:c.499_507del	ENSP00000508950.1:n.499_507del
ENST00000686888.1:c.*267_*275del	ENSP00000509619.1:n.*267_*275del
ENST00000687699.1:c.824_832del	ENSP00000508878.1:n.824_832del
ENST00000687786.1:n.2136_2144del
ENST00000688100.1:n.1621_1629del
ENST00000688588.1:c.700_708del	ENSP00000510802.1:p.Leu234_Val236del
ENST00000688927.1:n.2911_2919del
ENST00000689283.1:c.*363_*371del	ENSP00000509050.1:n.*363_*371del
ENST00000689477.1:c.*593_*601del	ENSP00000508945.1:n.*593_*601del
ENST00000689765.1:c.*193_*201del	ENSP00000509625.1:n.*193_*201del
ENST00000690512.1:c.*551_*559del	ENSP00000509793.1:n.*551_*559del
ENST00000692039.1:c.*498_*506del	ENSP00000508821.1:n.*498_*506del
ENST00000692336.1:c.724_732del	ENSP00000508540.1:p.Leu242_Val244del
ENST00000693133.1:n.1180_1188del
ENST00000263578.10:c.700_708del MANE Select	ENSP00000263578.5:p.Leu234_Val236del
ENST00000263578.9:c.700_708del	ENSP00000263578.5:p.Leu234_Val236del
ENST00000525083.5:n.420_428del
ENST00000525770.5:c.*332_*340del	ENSP00000434739.1:n.*332_*340del
ENST00000527004.5:c.*44_*52del	ENSP00000436374.1:n.*44_*52del
ENST00000530642.1:n.1482_1490del
ENST00000532101.5:n.923_931del
ENST00000532125.1:c.658_666del	ENSP00000434178.1:p.Leu220_Val222del
ENST00000533395.5:n.433_441del
ENST00000533839.5:n.238-399_238-391del
ENST00000534011.5:n.752_760del
ENST00000534315.5:n.1012_1020del
NM_017547.3:c.700_708del	NP_060017.1:p.Leu234_Val236del
NR_037647.1:n.646_654del
NR_037648.1:n.886_894del
XM_006718879.2:c.190_198del	XP_006718942.1:p.Leu64_Val66del
XM_006718880.2:c.67_75del	XP_006718943.1:p.Leu23_Val25del
XM_006718881.2:c.67_75del	XP_006718944.1:p.Leu23_Val25del
XM_011542895.1:c.190_198del	XP_011541197.1:p.Leu64_Val66del
XM_011542896.1:c.190_198del	XP_011541198.1:p.Leu64_Val66del
XM_006718879.3:c.190_198del	XP_006718942.1:p.Leu64_Val66del
XM_006718881.3:c.67_75del	XP_006718944.1:p.Leu23_Val25del
XM_011542895.2:c.190_198del	XP_011541197.1:p.Leu64_Val66del
XM_011542896.2:c.190_198del	XP_011541198.1:p.Leu64_Val66del
XM_017018000.2:c.700_708del	XP_016873489.1:p.Leu234_Val236del
XM_017018001.1:c.190_198del	XP_016873490.1:p.Leu64_Val66del
XM_017018002.1:c.190_198del	XP_016873491.1:p.Leu64_Val66del
XM_017018003.2:c.67_75del	XP_016873492.1:p.Leu23_Val25del
XM_017018004.1:c.67_75del	XP_016873493.1:p.Leu23_Val25del
XM_017018005.1:c.67_75del	XP_016873494.1:p.Leu23_Val25del
XM_017018006.2:c.67_75del	XP_016873495.1:p.Leu23_Val25del
NM_017547.4:c.700_708del MANE Select	NP_060017.1:p.Leu234_Val236del
NR_037647.2:n.532_540del
NR_037648.2:n.877_885del