Canonical Allele Identifier: CA6354170

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 303537
• ClinVar RCV Id: RCV000366903 ; RCV002522187
• dbSNP Id: rs753106152
• ExAC: 11:126145248 C / T
• gnomAD v2: 11-126145248-C-T
• gnomAD v3: 11-126275353-C-T
• gnomAD v4: 11-126275353-C-T
• MyVariant Identifiers: chr11:g.126145248C>T (hg19) ; chr11:g.126275353C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275353C>T , CM000673.2:g.126275353C>T	GRCh38
NC_000011.9:g.126145248C>T , CM000673.1:g.126145248C>T	GRCh37
NC_000011.8:g.125650458C>T	NCBI36
NG_028029.1:g.11314C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1141C>T
ENST00000532101.6:n.760C>T
ENST00000532125.2:c.655C>T	ENSP00000434178.2:p.Pro219Ser
ENST00000533839.6:c.86-441C>T	ENSP00000509952.1:n.86-441C>T
ENST00000534011.6:n.950C>T
ENST00000685484.1:c.658C>T	ENSP00000510622.1:p.Pro220Ser
ENST00000685601.1:c.658C>T	ENSP00000510603.1:p.Pro220Ser
ENST00000685765.1:c.658C>T	ENSP00000509991.1:p.Pro220Ser
ENST00000685844.1:c.*195C>T	ENSP00000509820.1:n.*195C>T
ENST00000685857.1:n.1397C>T
ENST00000686242.1:c.457C>T	ENSP00000508950.1:n.457C>T
ENST00000686888.1:c.*225C>T	ENSP00000509619.1:n.*225C>T
ENST00000687699.1:c.782C>T	ENSP00000508878.1:n.782C>T
ENST00000687786.1:n.2094C>T
ENST00000688100.1:n.1579C>T
ENST00000688588.1:c.658C>T	ENSP00000510802.1:p.Pro220Ser
ENST00000688927.1:n.2869C>T
ENST00000689283.1:c.*321C>T	ENSP00000509050.1:n.*321C>T
ENST00000689477.1:c.*551C>T	ENSP00000508945.1:n.*551C>T
ENST00000689765.1:c.*169-18C>T	ENSP00000509625.1:n.*169-18C>T
ENST00000690512.1:c.*509C>T	ENSP00000509793.1:n.*509C>T
ENST00000692039.1:c.*456C>T	ENSP00000508821.1:n.*456C>T
ENST00000692336.1:c.682C>T	ENSP00000508540.1:p.Pro228Ser
ENST00000693133.1:n.1138C>T
ENST00000263578.10:c.658C>T MANE Select	ENSP00000263578.5:p.Pro220Ser
ENST00000263578.9:c.658C>T	ENSP00000263578.5:p.Pro220Ser
ENST00000525083.5:n.378C>T
ENST00000525770.5:c.*290C>T	ENSP00000434739.1:n.*290C>T
ENST00000527004.5:c.*2C>T	ENSP00000436374.1:n.*2C>T
ENST00000530642.1:n.1440C>T
ENST00000532101.5:n.881C>T
ENST00000532125.1:c.616C>T	ENSP00000434178.1:p.Pro206Ser
ENST00000533395.5:n.391C>T
ENST00000533839.5:n.238-441C>T
ENST00000534011.5:n.710C>T
ENST00000534315.5:n.970C>T
NM_017547.3:c.658C>T	NP_060017.1:p.Pro220Ser
NR_037647.1:n.604C>T
NR_037648.1:n.844C>T
XM_006718879.2:c.148C>T	XP_006718942.1:p.Pro50Ser
XM_006718880.2:c.25C>T	XP_006718943.1:p.Pro9Ser
XM_006718881.2:c.25C>T	XP_006718944.1:p.Pro9Ser
XM_011542895.1:c.148C>T	XP_011541197.1:p.Pro50Ser
XM_011542896.1:c.148C>T	XP_011541198.1:p.Pro50Ser
XM_006718879.3:c.148C>T	XP_006718942.1:p.Pro50Ser
XM_006718881.3:c.25C>T	XP_006718944.1:p.Pro9Ser
XM_011542895.2:c.148C>T	XP_011541197.1:p.Pro50Ser
XM_011542896.2:c.148C>T	XP_011541198.1:p.Pro50Ser
XM_017018000.2:c.658C>T	XP_016873489.1:p.Pro220Ser
XM_017018001.1:c.148C>T	XP_016873490.1:p.Pro50Ser
XM_017018002.1:c.148C>T	XP_016873491.1:p.Pro50Ser
XM_017018003.2:c.25C>T	XP_016873492.1:p.Pro9Ser
XM_017018004.1:c.25C>T	XP_016873493.1:p.Pro9Ser
XM_017018005.1:c.25C>T	XP_016873494.1:p.Pro9Ser
XM_017018006.2:c.25C>T	XP_016873495.1:p.Pro9Ser
NM_017547.4:c.658C>T MANE Select	NP_060017.1:p.Pro220Ser
NR_037647.2:n.490C>T
NR_037648.2:n.835C>T