Canonical Allele Identifier: CA477516095

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145289C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275394C>T , CM000673.2:g.126275394C>T	GRCh38
NC_000011.9:g.126145289C>T , CM000673.1:g.126145289C>T	GRCh37
NC_000011.8:g.125650499C>T	NCBI36
NG_028029.1:g.11355C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1182C>T
ENST00000532101.6:n.801C>T
ENST00000532125.2:c.696C>T	ENSP00000434178.2:p.Ser232=
ENST00000533839.6:c.86-400C>T	ENSP00000509952.1:n.86-400C>T
ENST00000534011.6:n.991C>T
ENST00000685484.1:c.699C>T	ENSP00000510622.1:p.Ser233=
ENST00000685601.1:c.699C>T	ENSP00000510603.1:p.Ser233=
ENST00000685765.1:c.699C>T	ENSP00000509991.1:p.Ser233=
ENST00000685844.1:c.*236C>T	ENSP00000509820.1:n.*236C>T
ENST00000685857.1:n.1438C>T
ENST00000686242.1:c.498C>T	ENSP00000508950.1:n.498C>T
ENST00000686888.1:c.*266C>T	ENSP00000509619.1:n.*266C>T
ENST00000687699.1:c.823C>T	ENSP00000508878.1:n.823C>T
ENST00000687786.1:n.2135C>T
ENST00000688100.1:n.1620C>T
ENST00000688588.1:c.699C>T	ENSP00000510802.1:p.Ser233=
ENST00000688927.1:n.2910C>T
ENST00000689283.1:c.*362C>T	ENSP00000509050.1:n.*362C>T
ENST00000689477.1:c.*592C>T	ENSP00000508945.1:n.*592C>T
ENST00000689765.1:c.*192C>T	ENSP00000509625.1:n.*192C>T
ENST00000690512.1:c.*550C>T	ENSP00000509793.1:n.*550C>T
ENST00000692039.1:c.*497C>T	ENSP00000508821.1:n.*497C>T
ENST00000692336.1:c.723C>T	ENSP00000508540.1:p.Ser241=
ENST00000693133.1:n.1179C>T
ENST00000263578.10:c.699C>T MANE Select	ENSP00000263578.5:p.Ser233=
ENST00000263578.9:c.699C>T	ENSP00000263578.5:p.Ser233=
ENST00000525083.5:n.419C>T
ENST00000525770.5:c.*331C>T	ENSP00000434739.1:n.*331C>T
ENST00000527004.5:c.*43C>T	ENSP00000436374.1:n.*43C>T
ENST00000530642.1:n.1481C>T
ENST00000532101.5:n.922C>T
ENST00000532125.1:c.657C>T	ENSP00000434178.1:p.Ser219=
ENST00000533395.5:n.432C>T
ENST00000533839.5:n.238-400C>T
ENST00000534011.5:n.751C>T
ENST00000534315.5:n.1011C>T
NM_017547.3:c.699C>T	NP_060017.1:p.Ser233=
NR_037647.1:n.645C>T
NR_037648.1:n.885C>T
XM_006718879.2:c.189C>T	XP_006718942.1:p.Ser63=
XM_006718880.2:c.66C>T	XP_006718943.1:p.Ser22=
XM_006718881.2:c.66C>T	XP_006718944.1:p.Ser22=
XM_011542895.1:c.189C>T	XP_011541197.1:p.Ser63=
XM_011542896.1:c.189C>T	XP_011541198.1:p.Ser63=
XM_006718879.3:c.189C>T	XP_006718942.1:p.Ser63=
XM_006718881.3:c.66C>T	XP_006718944.1:p.Ser22=
XM_011542895.2:c.189C>T	XP_011541197.1:p.Ser63=
XM_011542896.2:c.189C>T	XP_011541198.1:p.Ser63=
XM_017018000.2:c.699C>T	XP_016873489.1:p.Ser233=
XM_017018001.1:c.189C>T	XP_016873490.1:p.Ser63=
XM_017018002.1:c.189C>T	XP_016873491.1:p.Ser63=
XM_017018003.2:c.66C>T	XP_016873492.1:p.Ser22=
XM_017018004.1:c.66C>T	XP_016873493.1:p.Ser22=
XM_017018005.1:c.66C>T	XP_016873494.1:p.Ser22=
XM_017018006.2:c.66C>T	XP_016873495.1:p.Ser22=
NM_017547.4:c.699C>T MANE Select	NP_060017.1:p.Ser233=
NR_037647.2:n.531C>T
NR_037648.2:n.876C>T