Canonical Allele Identifier: CA383230224

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145296G>T (hg19) ; chr11:g.126275401G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275401G>T , CM000673.2:g.126275401G>T	GRCh38
NC_000011.9:g.126145296G>T , CM000673.1:g.126145296G>T	GRCh37
NC_000011.8:g.125650506G>T	NCBI36
NG_028029.1:g.11362G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1189G>T
ENST00000532101.6:n.808G>T
ENST00000532125.2:c.703G>T	ENSP00000434178.2:p.Val235Phe
ENST00000533839.6:c.86-393G>T	ENSP00000509952.1:n.86-393G>T
ENST00000534011.6:n.998G>T
ENST00000685484.1:c.706G>T	ENSP00000510622.1:p.Val236Phe
ENST00000685601.1:c.706G>T	ENSP00000510603.1:p.Val236Phe
ENST00000685765.1:c.706G>T	ENSP00000509991.1:p.Val236Phe
ENST00000685844.1:c.*243G>T	ENSP00000509820.1:n.*243G>T
ENST00000685857.1:n.1445G>T
ENST00000686242.1:c.505G>T	ENSP00000508950.1:n.505G>T
ENST00000686888.1:c.*273G>T	ENSP00000509619.1:n.*273G>T
ENST00000687699.1:c.830G>T	ENSP00000508878.1:n.830G>T
ENST00000687786.1:n.2142G>T
ENST00000688100.1:n.1627G>T
ENST00000688588.1:c.706G>T	ENSP00000510802.1:p.Val236Phe
ENST00000688927.1:n.2917G>T
ENST00000689283.1:c.*369G>T	ENSP00000509050.1:n.*369G>T
ENST00000689477.1:c.*599G>T	ENSP00000508945.1:n.*599G>T
ENST00000689765.1:c.*199G>T	ENSP00000509625.1:n.*199G>T
ENST00000690512.1:c.*557G>T	ENSP00000509793.1:n.*557G>T
ENST00000692039.1:c.*504G>T	ENSP00000508821.1:n.*504G>T
ENST00000692336.1:c.730G>T	ENSP00000508540.1:p.Val244Phe
ENST00000693133.1:n.1186G>T
ENST00000263578.10:c.706G>T MANE Select	ENSP00000263578.5:p.Val236Phe
ENST00000263578.9:c.706G>T	ENSP00000263578.5:p.Val236Phe
ENST00000525083.5:n.426G>T
ENST00000525770.5:c.*338G>T	ENSP00000434739.1:n.*338G>T
ENST00000527004.5:c.*50G>T	ENSP00000436374.1:n.*50G>T
ENST00000530642.1:n.1488G>T
ENST00000532101.5:n.929G>T
ENST00000532125.1:c.664G>T	ENSP00000434178.1:p.Val222Phe
ENST00000533395.5:n.439G>T
ENST00000533839.5:n.238-393G>T
ENST00000534011.5:n.758G>T
ENST00000534315.5:n.1018G>T
NM_017547.3:c.706G>T	NP_060017.1:p.Val236Phe
NR_037647.1:n.652G>T
NR_037648.1:n.892G>T
XM_006718879.2:c.196G>T	XP_006718942.1:p.Val66Phe
XM_006718880.2:c.73G>T	XP_006718943.1:p.Val25Phe
XM_006718881.2:c.73G>T	XP_006718944.1:p.Val25Phe
XM_011542895.1:c.196G>T	XP_011541197.1:p.Val66Phe
XM_011542896.1:c.196G>T	XP_011541198.1:p.Val66Phe
XM_006718879.3:c.196G>T	XP_006718942.1:p.Val66Phe
XM_006718881.3:c.73G>T	XP_006718944.1:p.Val25Phe
XM_011542895.2:c.196G>T	XP_011541197.1:p.Val66Phe
XM_011542896.2:c.196G>T	XP_011541198.1:p.Val66Phe
XM_017018000.2:c.706G>T	XP_016873489.1:p.Val236Phe
XM_017018001.1:c.196G>T	XP_016873490.1:p.Val66Phe
XM_017018002.1:c.196G>T	XP_016873491.1:p.Val66Phe
XM_017018003.2:c.73G>T	XP_016873492.1:p.Val25Phe
XM_017018004.1:c.73G>T	XP_016873493.1:p.Val25Phe
XM_017018005.1:c.73G>T	XP_016873494.1:p.Val25Phe
XM_017018006.2:c.73G>T	XP_016873495.1:p.Val25Phe
NM_017547.4:c.706G>T MANE Select	NP_060017.1:p.Val236Phe
NR_037647.2:n.538G>T
NR_037648.2:n.883G>T