Canonical Allele Identifier: CA6354178

Gene: FOXRED1

Linked Data

• dbSNP Id: rs757274475
• ExAC: 11:126145294 G / T
• gnomAD v2: 11-126145294-G-T
• gnomAD v4: 11-126275399-G-T
• MyVariant Identifiers: chr11:g.126145294G>T (hg19) ; chr11:g.126275399G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275399G>T , CM000673.2:g.126275399G>T	GRCh38
NC_000011.9:g.126145294G>T , CM000673.1:g.126145294G>T	GRCh37
NC_000011.8:g.125650504G>T	NCBI36
NG_028029.1:g.11360G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1187G>T
ENST00000532101.6:n.806G>T
ENST00000532125.2:c.701G>T	ENSP00000434178.2:p.Gly234Val
ENST00000533839.6:c.86-395G>T	ENSP00000509952.1:n.86-395G>T
ENST00000534011.6:n.996G>T
ENST00000685484.1:c.704G>T	ENSP00000510622.1:p.Gly235Val
ENST00000685601.1:c.704G>T	ENSP00000510603.1:p.Gly235Val
ENST00000685765.1:c.704G>T	ENSP00000509991.1:p.Gly235Val
ENST00000685844.1:c.*241G>T	ENSP00000509820.1:n.*241G>T
ENST00000685857.1:n.1443G>T
ENST00000686242.1:c.503G>T	ENSP00000508950.1:n.503G>T
ENST00000686888.1:c.*271G>T	ENSP00000509619.1:n.*271G>T
ENST00000687699.1:c.828G>T	ENSP00000508878.1:n.828G>T
ENST00000687786.1:n.2140G>T
ENST00000688100.1:n.1625G>T
ENST00000688588.1:c.704G>T	ENSP00000510802.1:p.Gly235Val
ENST00000688927.1:n.2915G>T
ENST00000689283.1:c.*367G>T	ENSP00000509050.1:n.*367G>T
ENST00000689477.1:c.*597G>T	ENSP00000508945.1:n.*597G>T
ENST00000689765.1:c.*197G>T	ENSP00000509625.1:n.*197G>T
ENST00000690512.1:c.*555G>T	ENSP00000509793.1:n.*555G>T
ENST00000692039.1:c.*502G>T	ENSP00000508821.1:n.*502G>T
ENST00000692336.1:c.728G>T	ENSP00000508540.1:p.Gly243Val
ENST00000693133.1:n.1184G>T
ENST00000263578.10:c.704G>T MANE Select	ENSP00000263578.5:p.Gly235Val
ENST00000263578.9:c.704G>T	ENSP00000263578.5:p.Gly235Val
ENST00000525083.5:n.424G>T
ENST00000525770.5:c.*336G>T	ENSP00000434739.1:n.*336G>T
ENST00000527004.5:c.*48G>T	ENSP00000436374.1:n.*48G>T
ENST00000530642.1:n.1486G>T
ENST00000532101.5:n.927G>T
ENST00000532125.1:c.662G>T	ENSP00000434178.1:p.Gly221Val
ENST00000533395.5:n.437G>T
ENST00000533839.5:n.238-395G>T
ENST00000534011.5:n.756G>T
ENST00000534315.5:n.1016G>T
NM_017547.3:c.704G>T	NP_060017.1:p.Gly235Val
NR_037647.1:n.650G>T
NR_037648.1:n.890G>T
XM_006718879.2:c.194G>T	XP_006718942.1:p.Gly65Val
XM_006718880.2:c.71G>T	XP_006718943.1:p.Gly24Val
XM_006718881.2:c.71G>T	XP_006718944.1:p.Gly24Val
XM_011542895.1:c.194G>T	XP_011541197.1:p.Gly65Val
XM_011542896.1:c.194G>T	XP_011541198.1:p.Gly65Val
XM_006718879.3:c.194G>T	XP_006718942.1:p.Gly65Val
XM_006718881.3:c.71G>T	XP_006718944.1:p.Gly24Val
XM_011542895.2:c.194G>T	XP_011541197.1:p.Gly65Val
XM_011542896.2:c.194G>T	XP_011541198.1:p.Gly65Val
XM_017018000.2:c.704G>T	XP_016873489.1:p.Gly235Val
XM_017018001.1:c.194G>T	XP_016873490.1:p.Gly65Val
XM_017018002.1:c.194G>T	XP_016873491.1:p.Gly65Val
XM_017018003.2:c.71G>T	XP_016873492.1:p.Gly24Val
XM_017018004.1:c.71G>T	XP_016873493.1:p.Gly24Val
XM_017018005.1:c.71G>T	XP_016873494.1:p.Gly24Val
XM_017018006.2:c.71G>T	XP_016873495.1:p.Gly24Val
NM_017547.4:c.704G>T MANE Select	NP_060017.1:p.Gly235Val
NR_037647.2:n.536G>T
NR_037648.2:n.881G>T