Canonical Allele Identifier: CA477516088

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145280G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275385G>A , CM000673.2:g.126275385G>A	GRCh38
NC_000011.9:g.126145280G>A , CM000673.1:g.126145280G>A	GRCh37
NC_000011.8:g.125650490G>A	NCBI36
NG_028029.1:g.11346G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1173G>A
ENST00000532101.6:n.792G>A
ENST00000532125.2:c.687G>A	ENSP00000434178.2:p.Lys229=
ENST00000533839.6:c.86-409G>A	ENSP00000509952.1:n.86-409G>A
ENST00000534011.6:n.982G>A
ENST00000685484.1:c.690G>A	ENSP00000510622.1:p.Lys230=
ENST00000685601.1:c.690G>A	ENSP00000510603.1:p.Lys230=
ENST00000685765.1:c.690G>A	ENSP00000509991.1:p.Lys230=
ENST00000685844.1:c.*227G>A	ENSP00000509820.1:n.*227G>A
ENST00000685857.1:n.1429G>A
ENST00000686242.1:c.489G>A	ENSP00000508950.1:n.489G>A
ENST00000686888.1:c.*257G>A	ENSP00000509619.1:n.*257G>A
ENST00000687699.1:c.814G>A	ENSP00000508878.1:n.814G>A
ENST00000687786.1:n.2126G>A
ENST00000688100.1:n.1611G>A
ENST00000688588.1:c.690G>A	ENSP00000510802.1:p.Lys230=
ENST00000688927.1:n.2901G>A
ENST00000689283.1:c.*353G>A	ENSP00000509050.1:n.*353G>A
ENST00000689477.1:c.*583G>A	ENSP00000508945.1:n.*583G>A
ENST00000689765.1:c.*183G>A	ENSP00000509625.1:n.*183G>A
ENST00000690512.1:c.*541G>A	ENSP00000509793.1:n.*541G>A
ENST00000692039.1:c.*488G>A	ENSP00000508821.1:n.*488G>A
ENST00000692336.1:c.714G>A	ENSP00000508540.1:p.Lys238=
ENST00000693133.1:n.1170G>A
ENST00000263578.10:c.690G>A MANE Select	ENSP00000263578.5:p.Lys230=
ENST00000263578.9:c.690G>A	ENSP00000263578.5:p.Lys230=
ENST00000525083.5:n.410G>A
ENST00000525770.5:c.*322G>A	ENSP00000434739.1:n.*322G>A
ENST00000527004.5:c.*34G>A	ENSP00000436374.1:n.*34G>A
ENST00000530642.1:n.1472G>A
ENST00000532101.5:n.913G>A
ENST00000532125.1:c.648G>A	ENSP00000434178.1:p.Lys216=
ENST00000533395.5:n.423G>A
ENST00000533839.5:n.238-409G>A
ENST00000534011.5:n.742G>A
ENST00000534315.5:n.1002G>A
NM_017547.3:c.690G>A	NP_060017.1:p.Lys230=
NR_037647.1:n.636G>A
NR_037648.1:n.876G>A
XM_006718879.2:c.180G>A	XP_006718942.1:p.Lys60=
XM_006718880.2:c.57G>A	XP_006718943.1:p.Lys19=
XM_006718881.2:c.57G>A	XP_006718944.1:p.Lys19=
XM_011542895.1:c.180G>A	XP_011541197.1:p.Lys60=
XM_011542896.1:c.180G>A	XP_011541198.1:p.Lys60=
XM_006718879.3:c.180G>A	XP_006718942.1:p.Lys60=
XM_006718881.3:c.57G>A	XP_006718944.1:p.Lys19=
XM_011542895.2:c.180G>A	XP_011541197.1:p.Lys60=
XM_011542896.2:c.180G>A	XP_011541198.1:p.Lys60=
XM_017018000.2:c.690G>A	XP_016873489.1:p.Lys230=
XM_017018001.1:c.180G>A	XP_016873490.1:p.Lys60=
XM_017018002.1:c.180G>A	XP_016873491.1:p.Lys60=
XM_017018003.2:c.57G>A	XP_016873492.1:p.Lys19=
XM_017018004.1:c.57G>A	XP_016873493.1:p.Lys19=
XM_017018005.1:c.57G>A	XP_016873494.1:p.Lys19=
XM_017018006.2:c.57G>A	XP_016873495.1:p.Lys19=
NM_017547.4:c.690G>A MANE Select	NP_060017.1:p.Lys230=
NR_037647.2:n.522G>A
NR_037648.2:n.867G>A