Canonical Allele Identifier: CA383230139

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145252G>A (hg19) ; chr11:g.126275357G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275357G>A , CM000673.2:g.126275357G>A	GRCh38
NC_000011.9:g.126145252G>A , CM000673.1:g.126145252G>A	GRCh37
NC_000011.8:g.125650462G>A	NCBI36
NG_028029.1:g.11318G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1145G>A
ENST00000532101.6:n.764G>A
ENST00000532125.2:c.659G>A	ENSP00000434178.2:p.Trp220Ter
ENST00000533839.6:c.86-437G>A	ENSP00000509952.1:n.86-437G>A
ENST00000534011.6:n.954G>A
ENST00000685484.1:c.662G>A	ENSP00000510622.1:p.Trp221Ter
ENST00000685601.1:c.662G>A	ENSP00000510603.1:p.Trp221Ter
ENST00000685765.1:c.662G>A	ENSP00000509991.1:p.Trp221Ter
ENST00000685844.1:c.*199G>A	ENSP00000509820.1:n.*199G>A
ENST00000685857.1:n.1401G>A
ENST00000686242.1:c.461G>A	ENSP00000508950.1:n.461G>A
ENST00000686888.1:c.*229G>A	ENSP00000509619.1:n.*229G>A
ENST00000687699.1:c.786G>A	ENSP00000508878.1:n.786G>A
ENST00000687786.1:n.2098G>A
ENST00000688100.1:n.1583G>A
ENST00000688588.1:c.662G>A	ENSP00000510802.1:p.Trp221Ter
ENST00000688927.1:n.2873G>A
ENST00000689283.1:c.*325G>A	ENSP00000509050.1:n.*325G>A
ENST00000689477.1:c.*555G>A	ENSP00000508945.1:n.*555G>A
ENST00000689765.1:c.*169-14G>A	ENSP00000509625.1:n.*169-14G>A
ENST00000690512.1:c.*513G>A	ENSP00000509793.1:n.*513G>A
ENST00000692039.1:c.*460G>A	ENSP00000508821.1:n.*460G>A
ENST00000692336.1:c.686G>A	ENSP00000508540.1:p.Trp229Ter
ENST00000693133.1:n.1142G>A
ENST00000263578.10:c.662G>A MANE Select	ENSP00000263578.5:p.Trp221Ter
ENST00000263578.9:c.662G>A	ENSP00000263578.5:p.Trp221Ter
ENST00000525083.5:n.382G>A
ENST00000525770.5:c.*294G>A	ENSP00000434739.1:n.*294G>A
ENST00000527004.5:c.*6G>A	ENSP00000436374.1:n.*6G>A
ENST00000530642.1:n.1444G>A
ENST00000532101.5:n.885G>A
ENST00000532125.1:c.620G>A	ENSP00000434178.1:p.Trp207Ter
ENST00000533395.5:n.395G>A
ENST00000533839.5:n.238-437G>A
ENST00000534011.5:n.714G>A
ENST00000534315.5:n.974G>A
NM_017547.3:c.662G>A	NP_060017.1:p.Trp221Ter
NR_037647.1:n.608G>A
NR_037648.1:n.848G>A
XM_006718879.2:c.152G>A	XP_006718942.1:p.Trp51Ter
XM_006718880.2:c.29G>A	XP_006718943.1:p.Trp10Ter
XM_006718881.2:c.29G>A	XP_006718944.1:p.Trp10Ter
XM_011542895.1:c.152G>A	XP_011541197.1:p.Trp51Ter
XM_011542896.1:c.152G>A	XP_011541198.1:p.Trp51Ter
XM_006718879.3:c.152G>A	XP_006718942.1:p.Trp51Ter
XM_006718881.3:c.29G>A	XP_006718944.1:p.Trp10Ter
XM_011542895.2:c.152G>A	XP_011541197.1:p.Trp51Ter
XM_011542896.2:c.152G>A	XP_011541198.1:p.Trp51Ter
XM_017018000.2:c.662G>A	XP_016873489.1:p.Trp221Ter
XM_017018001.1:c.152G>A	XP_016873490.1:p.Trp51Ter
XM_017018002.1:c.152G>A	XP_016873491.1:p.Trp51Ter
XM_017018003.2:c.29G>A	XP_016873492.1:p.Trp10Ter
XM_017018004.1:c.29G>A	XP_016873493.1:p.Trp10Ter
XM_017018005.1:c.29G>A	XP_016873494.1:p.Trp10Ter
XM_017018006.2:c.29G>A	XP_016873495.1:p.Trp10Ter
NM_017547.4:c.662G>A MANE Select	NP_060017.1:p.Trp221Ter
NR_037647.2:n.494G>A
NR_037648.2:n.839G>A