Canonical Allele Identifier: CA477513639

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126141468T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271573T>C , CM000673.2:g.126271573T>C	GRCh38
NC_000011.9:g.126141468T>C , CM000673.1:g.126141468T>C	GRCh37
NC_000011.8:g.125646678T>C	NCBI36
NG_028029.1:g.7534T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.400T>C
ENST00000532101.6:n.399T>C
ENST00000532125.2:c.222T>C	ENSP00000434178.2:p.Leu74=
ENST00000533839.6:c.85+2282T>C	ENSP00000509952.1:n.85+2282T>C
ENST00000534011.6:n.498T>C
ENST00000685484.1:c.222T>C	ENSP00000510622.1:p.Leu74=
ENST00000685601.1:c.222T>C	ENSP00000510603.1:p.Leu74=
ENST00000685765.1:c.222T>C	ENSP00000509991.1:p.Leu74=
ENST00000685844.1:c.86-1396T>C	ENSP00000509820.1:n.86-1396T>C
ENST00000685857.1:n.400T>C
ENST00000686242.1:c.86-1396T>C	ENSP00000508950.1:n.86-1396T>C
ENST00000686888.1:c.222T>C	ENSP00000509619.1:p.Leu74=
ENST00000687699.1:c.346T>C	ENSP00000508878.1:n.346T>C
ENST00000687786.1:n.1555T>C
ENST00000688588.1:c.222T>C	ENSP00000510802.1:p.Leu74=
ENST00000688927.1:n.400T>C
ENST00000689283.1:c.210-1396T>C	ENSP00000509050.1:n.210-1396T>C
ENST00000689477.1:c.*115T>C	ENSP00000508945.1:n.*115T>C
ENST00000689765.1:c.86-1396T>C	ENSP00000509625.1:n.86-1396T>C
ENST00000690512.1:c.86-905T>C	ENSP00000509793.1:n.86-905T>C
ENST00000692039.1:c.*20T>C	ENSP00000508821.1:n.*20T>C
ENST00000692336.1:c.222T>C	ENSP00000508540.1:p.Leu74=
ENST00000693133.1:n.226-1396T>C
ENST00000263578.10:c.222T>C MANE Select	ENSP00000263578.5:p.Leu74=
ENST00000263578.9:c.222T>C	ENSP00000263578.5:p.Leu74=
ENST00000524751.5:n.223-1396T>C
ENST00000525083.5:n.122-1396T>C
ENST00000525770.5:c.86-1396T>C	ENSP00000434739.1:n.86-1396T>C
ENST00000526366.5:n.101-146T>C
ENST00000526525.1:n.246-1396T>C
ENST00000527004.5:c.222T>C	ENSP00000436374.1:p.Leu74=
ENST00000529802.1:n.272T>C
ENST00000532101.5:n.445T>C
ENST00000532125.1:c.180T>C	ENSP00000434178.1:p.Leu60=
ENST00000533839.5:n.237+2282T>C
ENST00000534011.5:n.158-905T>C
ENST00000534315.5:n.629T>C
NM_017547.3:c.222T>C	NP_060017.1:p.Leu74=
NR_037647.1:n.253-1396T>C
NR_037648.1:n.408T>C
XM_006718880.2:c.-317T>C	XP_006718943.1:n.-317T>C
XM_006718881.2:c.-232-1396T>C	XP_006718944.1:n.-232-1396T>C
XM_011542895.1:c.-289T>C	XP_011541197.1:n.-289T>C
XM_011542896.1:c.-309T>C	XP_011541198.1:n.-309T>C
XM_006718881.3:c.-232-1396T>C	XP_006718944.1:n.-232-1396T>C
XM_011542895.2:c.-289T>C	XP_011541197.1:n.-289T>C
XM_011542896.2:c.-309T>C	XP_011541198.1:n.-309T>C
XM_017018000.2:c.222T>C	XP_016873489.1:p.Leu74=
XM_017018001.1:c.-309T>C	XP_016873490.1:n.-309T>C
XM_017018002.1:c.-224-1396T>C	XP_016873491.1:n.-224-1396T>C
XM_017018003.2:c.-317T>C	XP_016873492.1:n.-317T>C
XM_017018004.1:c.-317T>C	XP_016873493.1:n.-317T>C
XM_017018005.1:c.-515T>C	XP_016873494.1:n.-515T>C
XM_017018006.2:c.-317T>C	XP_016873495.1:n.-317T>C
NM_017547.4:c.222T>C MANE Select	NP_060017.1:p.Leu74=
NR_037647.2:n.139-1396T>C
NR_037648.2:n.399T>C