Canonical Allele Identifier: CA477516099

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145295A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275400A>T , CM000673.2:g.126275400A>T	GRCh38
NC_000011.9:g.126145295A>T , CM000673.1:g.126145295A>T	GRCh37
NC_000011.8:g.125650505A>T	NCBI36
NG_028029.1:g.11361A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1188A>T
ENST00000532101.6:n.807A>T
ENST00000532125.2:c.702A>T	ENSP00000434178.2:p.Gly234=
ENST00000533839.6:c.86-394A>T	ENSP00000509952.1:n.86-394A>T
ENST00000534011.6:n.997A>T
ENST00000685484.1:c.705A>T	ENSP00000510622.1:p.Gly235=
ENST00000685601.1:c.705A>T	ENSP00000510603.1:p.Gly235=
ENST00000685765.1:c.705A>T	ENSP00000509991.1:p.Gly235=
ENST00000685844.1:c.*242A>T	ENSP00000509820.1:n.*242A>T
ENST00000685857.1:n.1444A>T
ENST00000686242.1:c.504A>T	ENSP00000508950.1:n.504A>T
ENST00000686888.1:c.*272A>T	ENSP00000509619.1:n.*272A>T
ENST00000687699.1:c.829A>T	ENSP00000508878.1:n.829A>T
ENST00000687786.1:n.2141A>T
ENST00000688100.1:n.1626A>T
ENST00000688588.1:c.705A>T	ENSP00000510802.1:p.Gly235=
ENST00000688927.1:n.2916A>T
ENST00000689283.1:c.*368A>T	ENSP00000509050.1:n.*368A>T
ENST00000689477.1:c.*598A>T	ENSP00000508945.1:n.*598A>T
ENST00000689765.1:c.*198A>T	ENSP00000509625.1:n.*198A>T
ENST00000690512.1:c.*556A>T	ENSP00000509793.1:n.*556A>T
ENST00000692039.1:c.*503A>T	ENSP00000508821.1:n.*503A>T
ENST00000692336.1:c.729A>T	ENSP00000508540.1:p.Gly243=
ENST00000693133.1:n.1185A>T
ENST00000263578.10:c.705A>T MANE Select	ENSP00000263578.5:p.Gly235=
ENST00000263578.9:c.705A>T	ENSP00000263578.5:p.Gly235=
ENST00000525083.5:n.425A>T
ENST00000525770.5:c.*337A>T	ENSP00000434739.1:n.*337A>T
ENST00000527004.5:c.*49A>T	ENSP00000436374.1:n.*49A>T
ENST00000530642.1:n.1487A>T
ENST00000532101.5:n.928A>T
ENST00000532125.1:c.663A>T	ENSP00000434178.1:p.Gly221=
ENST00000533395.5:n.438A>T
ENST00000533839.5:n.238-394A>T
ENST00000534011.5:n.757A>T
ENST00000534315.5:n.1017A>T
NM_017547.3:c.705A>T	NP_060017.1:p.Gly235=
NR_037647.1:n.651A>T
NR_037648.1:n.891A>T
XM_006718879.2:c.195A>T	XP_006718942.1:p.Gly65=
XM_006718880.2:c.72A>T	XP_006718943.1:p.Gly24=
XM_006718881.2:c.72A>T	XP_006718944.1:p.Gly24=
XM_011542895.1:c.195A>T	XP_011541197.1:p.Gly65=
XM_011542896.1:c.195A>T	XP_011541198.1:p.Gly65=
XM_006718879.3:c.195A>T	XP_006718942.1:p.Gly65=
XM_006718881.3:c.72A>T	XP_006718944.1:p.Gly24=
XM_011542895.2:c.195A>T	XP_011541197.1:p.Gly65=
XM_011542896.2:c.195A>T	XP_011541198.1:p.Gly65=
XM_017018000.2:c.705A>T	XP_016873489.1:p.Gly235=
XM_017018001.1:c.195A>T	XP_016873490.1:p.Gly65=
XM_017018002.1:c.195A>T	XP_016873491.1:p.Gly65=
XM_017018003.2:c.72A>T	XP_016873492.1:p.Gly24=
XM_017018004.1:c.72A>T	XP_016873493.1:p.Gly24=
XM_017018005.1:c.72A>T	XP_016873494.1:p.Gly24=
XM_017018006.2:c.72A>T	XP_016873495.1:p.Gly24=
NM_017547.4:c.705A>T MANE Select	NP_060017.1:p.Gly235=
NR_037647.2:n.537A>T
NR_037648.2:n.882A>T