Canonical Allele Identifier: CA383230187

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275381-G-T
• MyVariant Identifiers: chr11:g.126145276G>T (hg19) ; chr11:g.126275381G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275381G>T , CM000673.2:g.126275381G>T	GRCh38
NC_000011.9:g.126145276G>T , CM000673.1:g.126145276G>T	GRCh37
NC_000011.8:g.125650486G>T	NCBI36
NG_028029.1:g.11342G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1169G>T
ENST00000532101.6:n.788G>T
ENST00000532125.2:c.683G>T	ENSP00000434178.2:p.Arg228Leu
ENST00000533839.6:c.86-413G>T	ENSP00000509952.1:n.86-413G>T
ENST00000534011.6:n.978G>T
ENST00000685484.1:c.686G>T	ENSP00000510622.1:p.Arg229Leu
ENST00000685601.1:c.686G>T	ENSP00000510603.1:p.Arg229Leu
ENST00000685765.1:c.686G>T	ENSP00000509991.1:p.Arg229Leu
ENST00000685844.1:c.*223G>T	ENSP00000509820.1:n.*223G>T
ENST00000685857.1:n.1425G>T
ENST00000686242.1:c.485G>T	ENSP00000508950.1:n.485G>T
ENST00000686888.1:c.*253G>T	ENSP00000509619.1:n.*253G>T
ENST00000687699.1:c.810G>T	ENSP00000508878.1:n.810G>T
ENST00000687786.1:n.2122G>T
ENST00000688100.1:n.1607G>T
ENST00000688588.1:c.686G>T	ENSP00000510802.1:p.Arg229Leu
ENST00000688927.1:n.2897G>T
ENST00000689283.1:c.*349G>T	ENSP00000509050.1:n.*349G>T
ENST00000689477.1:c.*579G>T	ENSP00000508945.1:n.*579G>T
ENST00000689765.1:c.*179G>T	ENSP00000509625.1:n.*179G>T
ENST00000690512.1:c.*537G>T	ENSP00000509793.1:n.*537G>T
ENST00000692039.1:c.*484G>T	ENSP00000508821.1:n.*484G>T
ENST00000692336.1:c.710G>T	ENSP00000508540.1:p.Arg237Leu
ENST00000693133.1:n.1166G>T
ENST00000263578.10:c.686G>T MANE Select	ENSP00000263578.5:p.Arg229Leu
ENST00000263578.9:c.686G>T	ENSP00000263578.5:p.Arg229Leu
ENST00000525083.5:n.406G>T
ENST00000525770.5:c.*318G>T	ENSP00000434739.1:n.*318G>T
ENST00000527004.5:c.*30G>T	ENSP00000436374.1:n.*30G>T
ENST00000530642.1:n.1468G>T
ENST00000532101.5:n.909G>T
ENST00000532125.1:c.644G>T	ENSP00000434178.1:p.Arg215Leu
ENST00000533395.5:n.419G>T
ENST00000533839.5:n.238-413G>T
ENST00000534011.5:n.738G>T
ENST00000534315.5:n.998G>T
NM_017547.3:c.686G>T	NP_060017.1:p.Arg229Leu
NR_037647.1:n.632G>T
NR_037648.1:n.872G>T
XM_006718879.2:c.176G>T	XP_006718942.1:p.Arg59Leu
XM_006718880.2:c.53G>T	XP_006718943.1:p.Arg18Leu
XM_006718881.2:c.53G>T	XP_006718944.1:p.Arg18Leu
XM_011542895.1:c.176G>T	XP_011541197.1:p.Arg59Leu
XM_011542896.1:c.176G>T	XP_011541198.1:p.Arg59Leu
XM_006718879.3:c.176G>T	XP_006718942.1:p.Arg59Leu
XM_006718881.3:c.53G>T	XP_006718944.1:p.Arg18Leu
XM_011542895.2:c.176G>T	XP_011541197.1:p.Arg59Leu
XM_011542896.2:c.176G>T	XP_011541198.1:p.Arg59Leu
XM_017018000.2:c.686G>T	XP_016873489.1:p.Arg229Leu
XM_017018001.1:c.176G>T	XP_016873490.1:p.Arg59Leu
XM_017018002.1:c.176G>T	XP_016873491.1:p.Arg59Leu
XM_017018003.2:c.53G>T	XP_016873492.1:p.Arg18Leu
XM_017018004.1:c.53G>T	XP_016873493.1:p.Arg18Leu
XM_017018005.1:c.53G>T	XP_016873494.1:p.Arg18Leu
XM_017018006.2:c.53G>T	XP_016873495.1:p.Arg18Leu
NM_017547.4:c.686G>T MANE Select	NP_060017.1:p.Arg229Leu
NR_037647.2:n.518G>T
NR_037648.2:n.863G>T