Canonical Allele Identifier: CA2616727321

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126271237-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271237_126271238insT , CM000673.2:g.126271237_126271238insT	GRCh38
NC_000011.9:g.126141132_126141133insT , CM000673.1:g.126141132_126141133insT	GRCh37
NC_000011.8:g.125646342_125646343insT	NCBI36
NG_028029.1:g.7198_7199insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-200_264-199insT
ENST00000532101.6:n.63_64insT
ENST00000532125.2:c.86-200_86-199insT	ENSP00000434178.2:n.86-200_86-199insT
ENST00000533839.6:c.85+1946_85+1947insT	ENSP00000509952.1:n.85+1946_85+1947insT
ENST00000534011.6:n.162_163insT
ENST00000685484.1:c.86-200_86-199insT	ENSP00000510622.1:n.86-200_86-199insT
ENST00000685601.1:c.86-200_86-199insT	ENSP00000510603.1:n.86-200_86-199insT
ENST00000685765.1:c.86-200_86-199insT	ENSP00000509991.1:n.86-200_86-199insT
ENST00000685844.1:c.86-1732_86-1731insT	ENSP00000509820.1:n.86-1732_86-1731insT
ENST00000685857.1:n.264-200_264-199insT
ENST00000686242.1:c.86-1732_86-1731insT	ENSP00000508950.1:n.86-1732_86-1731insT
ENST00000686888.1:c.86-200_86-199insT	ENSP00000509619.1:n.86-200_86-199insT
ENST00000687699.1:c.210-200_210-199insT	ENSP00000508878.1:n.210-200_210-199insT
ENST00000687786.1:n.1219_1220insT
ENST00000688588.1:c.86-200_86-199insT	ENSP00000510802.1:n.86-200_86-199insT
ENST00000688927.1:n.264-200_264-199insT
ENST00000689283.1:c.210-1732_210-1731insT	ENSP00000509050.1:n.210-1732_210-1731insT
ENST00000689477.1:c.103_104insT	ENSP00000508945.1:p.Glu35ValfsTer4
ENST00000689765.1:c.86-1732_86-1731insT	ENSP00000509625.1:n.86-1732_86-1731insT
ENST00000690512.1:c.86-1241_86-1240insT	ENSP00000509793.1:n.86-1241_86-1240insT
ENST00000692039.1:c.86-114_86-113insT	ENSP00000508821.1:n.86-114_86-113insT
ENST00000692336.1:c.86-200_86-199insT	ENSP00000508540.1:n.86-200_86-199insT
ENST00000693133.1:n.226-1732_226-1731insT
ENST00000263578.10:c.86-200_86-199insT MANE Select	ENSP00000263578.5:n.86-200_86-199insT
ENST00000263578.9:c.86-200_86-199insT	ENSP00000263578.5:n.86-200_86-199insT
ENST00000524751.5:n.223-1732_223-1731insT
ENST00000525083.5:n.122-1732_122-1731insT
ENST00000525770.5:c.86-1732_86-1731insT	ENSP00000434739.1:n.86-1732_86-1731insT
ENST00000526366.5:n.101-482_101-481insT
ENST00000526525.1:n.246-1732_246-1731insT
ENST00000527004.5:c.86-200_86-199insT	ENSP00000436374.1:n.86-200_86-199insT
ENST00000529802.1:n.136-200_136-199insT
ENST00000532101.5:n.109_110insT
ENST00000532125.1:c.44-200_44-199insT	ENSP00000434178.1:n.44-200_44-199insT
ENST00000533839.5:n.237+1946_237+1947insT
ENST00000534011.5:n.158-1241_158-1240insT
ENST00000534315.5:n.293_294insT
NM_017547.3:c.86-200_86-199insT	NP_060017.1:n.86-200_86-199insT
NR_037647.1:n.253-1732_253-1731insT
NR_037648.1:n.272-200_272-199insT
XM_006718880.2:c.-653_-652insT	XP_006718943.1:n.-653_-652insT
XM_006718881.2:c.-232-1732_-232-1731insT	XP_006718944.1:n.-232-1732_-232-1731insT
XM_011542895.1:c.-625_-624insT	XP_011541197.1:n.-625_-624insT
XM_011542896.1:c.-445-200_-445-199insT	XP_011541198.1:n.-445-200_-445-199insT
XM_006718881.3:c.-232-1732_-232-1731insT	XP_006718944.1:n.-232-1732_-232-1731insT
XM_011542895.2:c.-625_-624insT	XP_011541197.1:n.-625_-624insT
XM_011542896.2:c.-445-200_-445-199insT	XP_011541198.1:n.-445-200_-445-199insT
XM_017018000.2:c.86-200_86-199insT	XP_016873489.1:n.86-200_86-199insT
XM_017018001.1:c.-445-200_-445-199insT	XP_016873490.1:n.-445-200_-445-199insT
XM_017018002.1:c.-224-1732_-224-1731insT	XP_016873491.1:n.-224-1732_-224-1731insT
XM_017018003.2:c.-453-200_-453-199insT	XP_016873492.1:n.-453-200_-453-199insT
XM_017018004.1:c.-653_-652insT	XP_016873493.1:n.-653_-652insT
XM_017018005.1:c.-851_-850insT	XP_016873494.1:n.-851_-850insT
XM_017018006.2:c.-453-200_-453-199insT	XP_016873495.1:n.-453-200_-453-199insT
NM_017547.4:c.86-200_86-199insT MANE Select	NP_060017.1:n.86-200_86-199insT
NR_037647.2:n.139-1732_139-1731insT
NR_037648.2:n.263-200_263-199insT