Canonical Allele Identifier: CA2603837532

Gene: FOXRED1

Linked Data

• gnomAD v3: 11-126271202-GGAAATTGAATCTTGCAGTGCTTGGCACAATGCAT-G
• gnomAD v4: 11-126271202-GGAAATTGAATCTTGCAGTGCTTGGCACAATGCAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271206_126271239del , CM000673.2:g.126271206_126271239del	GRCh38
NC_000011.9:g.126141101_126141134del , CM000673.1:g.126141101_126141134del	GRCh37
NC_000011.8:g.125646311_125646344del	NCBI36
NG_028029.1:g.7167_7200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-231_264-198del
ENST00000532101.6:n.46-14_65del
ENST00000532125.2:c.86-231_86-198del	ENSP00000434178.2:n.86-231_86-198del
ENST00000533839.6:c.85+1915_85+1948del	ENSP00000509952.1:n.85+1915_85+1948del
ENST00000534011.6:n.145-14_164del
ENST00000685484.1:c.86-231_86-198del	ENSP00000510622.1:n.86-231_86-198del
ENST00000685601.1:c.86-231_86-198del	ENSP00000510603.1:n.86-231_86-198del
ENST00000685765.1:c.86-231_86-198del	ENSP00000509991.1:n.86-231_86-198del
ENST00000685844.1:c.86-1763_86-1730del	ENSP00000509820.1:n.86-1763_86-1730del
ENST00000685857.1:n.264-231_264-198del
ENST00000686242.1:c.86-1763_86-1730del	ENSP00000508950.1:n.86-1763_86-1730del
ENST00000686888.1:c.86-231_86-198del	ENSP00000509619.1:n.86-231_86-198del
ENST00000687699.1:c.210-231_210-198del	ENSP00000508878.1:n.210-231_210-198del
ENST00000687786.1:n.1188_1221del
ENST00000688588.1:c.86-231_86-198del	ENSP00000510802.1:n.86-231_86-198del
ENST00000688927.1:n.264-231_264-198del
ENST00000689283.1:c.210-1763_210-1730del	ENSP00000509050.1:n.210-1763_210-1730del
ENST00000689477.1:c.86-14_105del
ENST00000689765.1:c.86-1763_86-1730del	ENSP00000509625.1:n.86-1763_86-1730del
ENST00000690512.1:c.86-1272_86-1239del	ENSP00000509793.1:n.86-1272_86-1239del
ENST00000692039.1:c.86-145_86-112del	ENSP00000508821.1:n.86-145_86-112del
ENST00000692336.1:c.86-231_86-198del	ENSP00000508540.1:n.86-231_86-198del
ENST00000693133.1:n.226-1763_226-1730del
ENST00000263578.10:c.86-231_86-198del MANE Select	ENSP00000263578.5:n.86-231_86-198del
ENST00000263578.9:c.86-231_86-198del	ENSP00000263578.5:n.86-231_86-198del
ENST00000524751.5:n.223-1763_223-1730del
ENST00000525083.5:n.122-1763_122-1730del
ENST00000525770.5:c.86-1763_86-1730del	ENSP00000434739.1:n.86-1763_86-1730del
ENST00000526366.5:n.101-513_101-480del
ENST00000526525.1:n.246-1763_246-1730del
ENST00000527004.5:c.86-231_86-198del	ENSP00000436374.1:n.86-231_86-198del
ENST00000529802.1:n.136-231_136-198del
ENST00000532101.5:n.92-14_111del
ENST00000532125.1:c.44-231_44-198del	ENSP00000434178.1:n.44-231_44-198del
ENST00000533839.5:n.237+1915_237+1948del
ENST00000534011.5:n.158-1272_158-1239del
ENST00000534315.5:n.262_295del
NM_017547.3:c.86-231_86-198del	NP_060017.1:n.86-231_86-198del
NR_037647.1:n.253-1763_253-1730del
NR_037648.1:n.272-231_272-198del
XM_006718880.2:c.-684_-651del	XP_006718943.1:n.-684_-651del
XM_006718881.2:c.-232-1763_-232-1730del	XP_006718944.1:n.-232-1763_-232-1730del
XM_011542895.1:c.-642-14_-623del
XM_011542896.1:c.-445-231_-445-198del	XP_011541198.1:n.-445-231_-445-198del
XM_006718881.3:c.-232-1763_-232-1730del	XP_006718944.1:n.-232-1763_-232-1730del
XM_011542895.2:c.-642-14_-623del
XM_011542896.2:c.-445-231_-445-198del	XP_011541198.1:n.-445-231_-445-198del
XM_017018000.2:c.86-231_86-198del	XP_016873489.1:n.86-231_86-198del
XM_017018001.1:c.-445-231_-445-198del	XP_016873490.1:n.-445-231_-445-198del
XM_017018002.1:c.-224-1763_-224-1730del	XP_016873491.1:n.-224-1763_-224-1730del
XM_017018003.2:c.-453-231_-453-198del	XP_016873492.1:n.-453-231_-453-198del
XM_017018004.1:c.-670-14_-651del
XM_017018005.1:c.-882_-849del	XP_016873494.1:n.-882_-849del
XM_017018006.2:c.-453-231_-453-198del	XP_016873495.1:n.-453-231_-453-198del
NM_017547.4:c.86-231_86-198del MANE Select	NP_060017.1:n.86-231_86-198del
NR_037647.2:n.139-1763_139-1730del
NR_037648.2:n.263-231_263-198del