Canonical Allele Identifier: CA383230214

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145290T>A (hg19) ; chr11:g.126275395T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275395T>A , CM000673.2:g.126275395T>A	GRCh38
NC_000011.9:g.126145290T>A , CM000673.1:g.126145290T>A	GRCh37
NC_000011.8:g.125650500T>A	NCBI36
NG_028029.1:g.11356T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1183T>A
ENST00000532101.6:n.802T>A
ENST00000532125.2:c.697T>A	ENSP00000434178.2:p.Leu233Met
ENST00000533839.6:c.86-399T>A	ENSP00000509952.1:n.86-399T>A
ENST00000534011.6:n.992T>A
ENST00000685484.1:c.700T>A	ENSP00000510622.1:p.Leu234Met
ENST00000685601.1:c.700T>A	ENSP00000510603.1:p.Leu234Met
ENST00000685765.1:c.700T>A	ENSP00000509991.1:p.Leu234Met
ENST00000685844.1:c.*237T>A	ENSP00000509820.1:n.*237T>A
ENST00000685857.1:n.1439T>A
ENST00000686242.1:c.499T>A	ENSP00000508950.1:n.499T>A
ENST00000686888.1:c.*267T>A	ENSP00000509619.1:n.*267T>A
ENST00000687699.1:c.824T>A	ENSP00000508878.1:n.824T>A
ENST00000687786.1:n.2136T>A
ENST00000688100.1:n.1621T>A
ENST00000688588.1:c.700T>A	ENSP00000510802.1:p.Leu234Met
ENST00000688927.1:n.2911T>A
ENST00000689283.1:c.*363T>A	ENSP00000509050.1:n.*363T>A
ENST00000689477.1:c.*593T>A	ENSP00000508945.1:n.*593T>A
ENST00000689765.1:c.*193T>A	ENSP00000509625.1:n.*193T>A
ENST00000690512.1:c.*551T>A	ENSP00000509793.1:n.*551T>A
ENST00000692039.1:c.*498T>A	ENSP00000508821.1:n.*498T>A
ENST00000692336.1:c.724T>A	ENSP00000508540.1:p.Leu242Met
ENST00000693133.1:n.1180T>A
ENST00000263578.10:c.700T>A MANE Select	ENSP00000263578.5:p.Leu234Met
ENST00000263578.9:c.700T>A	ENSP00000263578.5:p.Leu234Met
ENST00000525083.5:n.420T>A
ENST00000525770.5:c.*332T>A	ENSP00000434739.1:n.*332T>A
ENST00000527004.5:c.*44T>A	ENSP00000436374.1:n.*44T>A
ENST00000530642.1:n.1482T>A
ENST00000532101.5:n.923T>A
ENST00000532125.1:c.658T>A	ENSP00000434178.1:p.Leu220Met
ENST00000533395.5:n.433T>A
ENST00000533839.5:n.238-399T>A
ENST00000534011.5:n.752T>A
ENST00000534315.5:n.1012T>A
NM_017547.3:c.700T>A	NP_060017.1:p.Leu234Met
NR_037647.1:n.646T>A
NR_037648.1:n.886T>A
XM_006718879.2:c.190T>A	XP_006718942.1:p.Leu64Met
XM_006718880.2:c.67T>A	XP_006718943.1:p.Leu23Met
XM_006718881.2:c.67T>A	XP_006718944.1:p.Leu23Met
XM_011542895.1:c.190T>A	XP_011541197.1:p.Leu64Met
XM_011542896.1:c.190T>A	XP_011541198.1:p.Leu64Met
XM_006718879.3:c.190T>A	XP_006718942.1:p.Leu64Met
XM_006718881.3:c.67T>A	XP_006718944.1:p.Leu23Met
XM_011542895.2:c.190T>A	XP_011541197.1:p.Leu64Met
XM_011542896.2:c.190T>A	XP_011541198.1:p.Leu64Met
XM_017018000.2:c.700T>A	XP_016873489.1:p.Leu234Met
XM_017018001.1:c.190T>A	XP_016873490.1:p.Leu64Met
XM_017018002.1:c.190T>A	XP_016873491.1:p.Leu64Met
XM_017018003.2:c.67T>A	XP_016873492.1:p.Leu23Met
XM_017018004.1:c.67T>A	XP_016873493.1:p.Leu23Met
XM_017018005.1:c.67T>A	XP_016873494.1:p.Leu23Met
XM_017018006.2:c.67T>A	XP_016873495.1:p.Leu23Met
NM_017547.4:c.700T>A MANE Select	NP_060017.1:p.Leu234Met
NR_037647.2:n.532T>A
NR_037648.2:n.877T>A