Canonical Allele Identifier: CA383230070

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275327-G-A
• MyVariant Identifiers: chr11:g.126145222G>A (hg19) ; chr11:g.126275327G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275327G>A , CM000673.2:g.126275327G>A	GRCh38
NC_000011.9:g.126145222G>A , CM000673.1:g.126145222G>A	GRCh37
NC_000011.8:g.125650432G>A	NCBI36
NG_028029.1:g.11288G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1115G>A
ENST00000532101.6:n.734G>A
ENST00000532125.2:c.629G>A	ENSP00000434178.2:p.Gly210Glu
ENST00000533839.6:c.86-467G>A	ENSP00000509952.1:n.86-467G>A
ENST00000534011.6:n.924G>A
ENST00000685484.1:c.632G>A	ENSP00000510622.1:p.Gly211Glu
ENST00000685601.1:c.632G>A	ENSP00000510603.1:p.Gly211Glu
ENST00000685765.1:c.632G>A	ENSP00000509991.1:p.Gly211Glu
ENST00000685844.1:c.*169G>A	ENSP00000509820.1:n.*169G>A
ENST00000685857.1:n.1371G>A
ENST00000686242.1:c.431G>A	ENSP00000508950.1:n.431G>A
ENST00000686888.1:c.*199G>A	ENSP00000509619.1:n.*199G>A
ENST00000687699.1:c.756G>A	ENSP00000508878.1:n.756G>A
ENST00000687786.1:n.2068G>A
ENST00000688100.1:n.1553G>A
ENST00000688588.1:c.632G>A	ENSP00000510802.1:p.Gly211Glu
ENST00000688927.1:n.2843G>A
ENST00000689283.1:c.*295G>A	ENSP00000509050.1:n.*295G>A
ENST00000689477.1:c.*525G>A	ENSP00000508945.1:n.*525G>A
ENST00000689765.1:c.*169-44G>A	ENSP00000509625.1:n.*169-44G>A
ENST00000690512.1:c.*483G>A	ENSP00000509793.1:n.*483G>A
ENST00000692039.1:c.*430G>A	ENSP00000508821.1:n.*430G>A
ENST00000692336.1:c.656G>A	ENSP00000508540.1:p.Gly219Glu
ENST00000693133.1:n.1112G>A
ENST00000263578.10:c.632G>A MANE Select	ENSP00000263578.5:p.Gly211Glu
ENST00000263578.9:c.632G>A	ENSP00000263578.5:p.Gly211Glu
ENST00000524751.5:n.873G>A
ENST00000525083.5:n.352G>A
ENST00000525770.5:c.*264G>A	ENSP00000434739.1:n.*264G>A
ENST00000527004.5:c.534G>A	ENSP00000436374.1:p.Arg178=
ENST00000530642.1:n.1414G>A
ENST00000532101.5:n.855G>A
ENST00000532125.1:c.590G>A	ENSP00000434178.1:p.Gly197Glu
ENST00000533395.5:n.365G>A
ENST00000533839.5:n.238-467G>A
ENST00000534011.5:n.684G>A
ENST00000534315.5:n.944G>A
NM_017547.3:c.632G>A	NP_060017.1:p.Gly211Glu
NR_037647.1:n.578G>A
NR_037648.1:n.818G>A
XM_006718879.2:c.122G>A	XP_006718942.1:p.Gly41Glu
XM_006718880.2:c.-2G>A	XP_006718943.1:n.-2G>A
XM_006718881.2:c.-2G>A	XP_006718944.1:n.-2G>A
XM_011542895.1:c.122G>A	XP_011541197.1:p.Gly41Glu
XM_011542896.1:c.122G>A	XP_011541198.1:p.Gly41Glu
XM_006718879.3:c.122G>A	XP_006718942.1:p.Gly41Glu
XM_006718881.3:c.-2G>A	XP_006718944.1:n.-2G>A
XM_011542895.2:c.122G>A	XP_011541197.1:p.Gly41Glu
XM_011542896.2:c.122G>A	XP_011541198.1:p.Gly41Glu
XM_017018000.2:c.632G>A	XP_016873489.1:p.Gly211Glu
XM_017018001.1:c.122G>A	XP_016873490.1:p.Gly41Glu
XM_017018002.1:c.122G>A	XP_016873491.1:p.Gly41Glu
XM_017018003.2:c.-2G>A	XP_016873492.1:n.-2G>A
XM_017018004.1:c.-2G>A	XP_016873493.1:n.-2G>A
XM_017018005.1:c.-2G>A	XP_016873494.1:n.-2G>A
XM_017018006.2:c.-2G>A	XP_016873495.1:n.-2G>A
NM_017547.4:c.632G>A MANE Select	NP_060017.1:p.Gly211Glu
NR_037647.2:n.464G>A
NR_037648.2:n.809G>A