Canonical Allele Identifier: CA2616727350

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126271239-A-AAATG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271239_126271240insAATG , CM000673.2:g.126271239_126271240insAATG	GRCh38
NC_000011.9:g.126141134_126141135insAATG , CM000673.1:g.126141134_126141135insAATG	GRCh37
NC_000011.8:g.125646344_125646345insAATG	NCBI36
NG_028029.1:g.7200_7201insAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-198_264-197insAATG
ENST00000532101.6:n.65_66insAATG
ENST00000532125.2:c.86-198_86-197insAATG	ENSP00000434178.2:n.86-198_86-197insAATG
ENST00000533839.6:c.85+1948_85+1949insAATG	ENSP00000509952.1:n.85+1948_85+1949insAATG
ENST00000534011.6:n.164_165insAATG
ENST00000685484.1:c.86-198_86-197insAATG	ENSP00000510622.1:n.86-198_86-197insAATG
ENST00000685601.1:c.86-198_86-197insAATG	ENSP00000510603.1:n.86-198_86-197insAATG
ENST00000685765.1:c.86-198_86-197insAATG	ENSP00000509991.1:n.86-198_86-197insAATG
ENST00000685844.1:c.86-1730_86-1729insAATG	ENSP00000509820.1:n.86-1730_86-1729insAATG
ENST00000685857.1:n.264-198_264-197insAATG
ENST00000686242.1:c.86-1730_86-1729insAATG	ENSP00000508950.1:n.86-1730_86-1729insAATG
ENST00000686888.1:c.86-198_86-197insAATG	ENSP00000509619.1:n.86-198_86-197insAATG
ENST00000687699.1:c.210-198_210-197insAATG	ENSP00000508878.1:n.210-198_210-197insAATG
ENST00000687786.1:n.1221_1222insAATG
ENST00000688588.1:c.86-198_86-197insAATG	ENSP00000510802.1:n.86-198_86-197insAATG
ENST00000688927.1:n.264-198_264-197insAATG
ENST00000689283.1:c.210-1730_210-1729insAATG	ENSP00000509050.1:n.210-1730_210-1729insAATG
ENST00000689477.1:c.105_106insAATG	ENSP00000508945.1:p.Glu36AsnfsTer4
ENST00000689765.1:c.86-1730_86-1729insAATG	ENSP00000509625.1:n.86-1730_86-1729insAATG
ENST00000690512.1:c.86-1239_86-1238insAATG	ENSP00000509793.1:n.86-1239_86-1238insAATG
ENST00000692039.1:c.86-112_86-111insAATG	ENSP00000508821.1:n.86-112_86-111insAATG
ENST00000692336.1:c.86-198_86-197insAATG	ENSP00000508540.1:n.86-198_86-197insAATG
ENST00000693133.1:n.226-1730_226-1729insAATG
ENST00000263578.10:c.86-198_86-197insAATG MANE Select	ENSP00000263578.5:n.86-198_86-197insAATG
ENST00000263578.9:c.86-198_86-197insAATG	ENSP00000263578.5:n.86-198_86-197insAATG
ENST00000524751.5:n.223-1730_223-1729insAATG
ENST00000525083.5:n.122-1730_122-1729insAATG
ENST00000525770.5:c.86-1730_86-1729insAATG	ENSP00000434739.1:n.86-1730_86-1729insAATG
ENST00000526366.5:n.101-480_101-479insAATG
ENST00000526525.1:n.246-1730_246-1729insAATG
ENST00000527004.5:c.86-198_86-197insAATG	ENSP00000436374.1:n.86-198_86-197insAATG
ENST00000529802.1:n.136-198_136-197insAATG
ENST00000532101.5:n.111_112insAATG
ENST00000532125.1:c.44-198_44-197insAATG	ENSP00000434178.1:n.44-198_44-197insAATG
ENST00000533839.5:n.237+1948_237+1949insAATG
ENST00000534011.5:n.158-1239_158-1238insAATG
ENST00000534315.5:n.295_296insAATG
NM_017547.3:c.86-198_86-197insAATG	NP_060017.1:n.86-198_86-197insAATG
NR_037647.1:n.253-1730_253-1729insAATG
NR_037648.1:n.272-198_272-197insAATG
XM_006718880.2:c.-651_-650insAATG	XP_006718943.1:n.-651_-650insAATG
XM_006718881.2:c.-232-1730_-232-1729insAATG	XP_006718944.1:n.-232-1730_-232-1729insAATG
XM_011542895.1:c.-623_-622insAATG	XP_011541197.1:n.-623_-622insAATG
XM_011542896.1:c.-445-198_-445-197insAATG	XP_011541198.1:n.-445-198_-445-197insAATG
XM_006718881.3:c.-232-1730_-232-1729insAATG	XP_006718944.1:n.-232-1730_-232-1729insAATG
XM_011542895.2:c.-623_-622insAATG	XP_011541197.1:n.-623_-622insAATG
XM_011542896.2:c.-445-198_-445-197insAATG	XP_011541198.1:n.-445-198_-445-197insAATG
XM_017018000.2:c.86-198_86-197insAATG	XP_016873489.1:n.86-198_86-197insAATG
XM_017018001.1:c.-445-198_-445-197insAATG	XP_016873490.1:n.-445-198_-445-197insAATG
XM_017018002.1:c.-224-1730_-224-1729insAATG	XP_016873491.1:n.-224-1730_-224-1729insAATG
XM_017018003.2:c.-453-198_-453-197insAATG	XP_016873492.1:n.-453-198_-453-197insAATG
XM_017018004.1:c.-651_-650insAATG	XP_016873493.1:n.-651_-650insAATG
XM_017018005.1:c.-849_-848insAATG	XP_016873494.1:n.-849_-848insAATG
XM_017018006.2:c.-453-198_-453-197insAATG	XP_016873495.1:n.-453-198_-453-197insAATG
NM_017547.4:c.86-198_86-197insAATG MANE Select	NP_060017.1:n.86-198_86-197insAATG
NR_037647.2:n.139-1730_139-1729insAATG
NR_037648.2:n.263-198_263-197insAATG