Canonical Allele Identifier: CA2616722584

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275517-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275517G>T , CM000673.2:g.126275517G>T	GRCh38
NC_000011.9:g.126145412G>T , CM000673.1:g.126145412G>T	GRCh37
NC_000011.8:g.125650622G>T	NCBI36
NG_028029.1:g.11478G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1216+89G>T
ENST00000532101.6:n.835+89G>T
ENST00000532125.2:c.730+89G>T	ENSP00000434178.2:n.730+89G>T
ENST00000533839.6:c.86-277G>T	ENSP00000509952.1:n.86-277G>T
ENST00000534011.6:n.1025+89G>T
ENST00000685484.1:c.733+89G>T	ENSP00000510622.1:n.733+89G>T
ENST00000685601.1:c.733+89G>T	ENSP00000510603.1:n.733+89G>T
ENST00000685765.1:c.733+89G>T	ENSP00000509991.1:n.733+89G>T
ENST00000685844.1:c.*270+89G>T	ENSP00000509820.1:n.*270+89G>T
ENST00000685857.1:n.1561G>T
ENST00000686242.1:c.532+89G>T	ENSP00000508950.1:n.532+89G>T
ENST00000686888.1:c.*300+89G>T	ENSP00000509619.1:n.*300+89G>T
ENST00000687699.1:c.857+89G>T	ENSP00000508878.1:n.857+89G>T
ENST00000687786.1:n.2169+89G>T
ENST00000688100.1:n.1654+89G>T
ENST00000688588.1:c.733+89G>T	ENSP00000510802.1:n.733+89G>T
ENST00000688927.1:n.2944+89G>T
ENST00000689283.1:c.*396+89G>T	ENSP00000509050.1:n.*396+89G>T
ENST00000689477.1:c.*626+89G>T	ENSP00000508945.1:n.*626+89G>T
ENST00000689765.1:c.*226+89G>T	ENSP00000509625.1:n.*226+89G>T
ENST00000690512.1:c.*584+89G>T	ENSP00000509793.1:n.*584+89G>T
ENST00000692039.1:c.*531+89G>T	ENSP00000508821.1:n.*531+89G>T
ENST00000692336.1:c.757+89G>T	ENSP00000508540.1:n.757+89G>T
ENST00000693133.1:n.1302G>T
ENST00000263578.10:c.733+89G>T MANE Select	ENSP00000263578.5:n.733+89G>T
ENST00000263578.9:c.733+89G>T	ENSP00000263578.5:n.733+89G>T
ENST00000525083.5:n.453+89G>T
ENST00000525770.5:c.*365+89G>T	ENSP00000434739.1:n.*365+89G>T
ENST00000527004.5:c.*77+89G>T	ENSP00000436374.1:n.*77+89G>T
ENST00000530642.1:n.1604G>T
ENST00000532101.5:n.956+89G>T
ENST00000532125.1:c.691+89G>T	ENSP00000434178.1:n.691+89G>T
ENST00000533395.5:n.466+89G>T
ENST00000533839.5:n.238-277G>T
ENST00000534011.5:n.785+89G>T
ENST00000534315.5:n.1045+89G>T
NM_017547.3:c.733+89G>T	NP_060017.1:n.733+89G>T
NR_037647.1:n.679+89G>T
NR_037648.1:n.919+89G>T
XM_006718879.2:c.223+89G>T	XP_006718942.1:n.223+89G>T
XM_006718880.2:c.100+89G>T	XP_006718943.1:n.100+89G>T
XM_006718881.2:c.100+89G>T	XP_006718944.1:n.100+89G>T
XM_011542895.1:c.223+89G>T	XP_011541197.1:n.223+89G>T
XM_011542896.1:c.223+89G>T	XP_011541198.1:n.223+89G>T
XM_006718879.3:c.223+89G>T	XP_006718942.1:n.223+89G>T
XM_006718881.3:c.100+89G>T	XP_006718944.1:n.100+89G>T
XM_011542895.2:c.223+89G>T	XP_011541197.1:n.223+89G>T
XM_011542896.2:c.223+89G>T	XP_011541198.1:n.223+89G>T
XM_017018000.2:c.733+89G>T	XP_016873489.1:n.733+89G>T
XM_017018001.1:c.223+89G>T	XP_016873490.1:n.223+89G>T
XM_017018002.1:c.223+89G>T	XP_016873491.1:n.223+89G>T
XM_017018003.2:c.100+89G>T	XP_016873492.1:n.100+89G>T
XM_017018004.1:c.100+89G>T	XP_016873493.1:n.100+89G>T
XM_017018005.1:c.100+89G>T	XP_016873494.1:n.100+89G>T
XM_017018006.2:c.100+89G>T	XP_016873495.1:n.100+89G>T
NM_017547.4:c.733+89G>T MANE Select	NP_060017.1:n.733+89G>T
NR_037647.2:n.565+89G>T
NR_037648.2:n.910+89G>T