Canonical Allele Identifier: CA477516041

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145256T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275361T>C , CM000673.2:g.126275361T>C	GRCh38
NC_000011.9:g.126145256T>C , CM000673.1:g.126145256T>C	GRCh37
NC_000011.8:g.125650466T>C	NCBI36
NG_028029.1:g.11322T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1149T>C
ENST00000532101.6:n.768T>C
ENST00000532125.2:c.663T>C	ENSP00000434178.2:p.Cys221=
ENST00000533839.6:c.86-433T>C	ENSP00000509952.1:n.86-433T>C
ENST00000534011.6:n.958T>C
ENST00000685484.1:c.666T>C	ENSP00000510622.1:p.Cys222=
ENST00000685601.1:c.666T>C	ENSP00000510603.1:p.Cys222=
ENST00000685765.1:c.666T>C	ENSP00000509991.1:p.Cys222=
ENST00000685844.1:c.*203T>C	ENSP00000509820.1:n.*203T>C
ENST00000685857.1:n.1405T>C
ENST00000686242.1:c.465T>C	ENSP00000508950.1:n.465T>C
ENST00000686888.1:c.*233T>C	ENSP00000509619.1:n.*233T>C
ENST00000687699.1:c.790T>C	ENSP00000508878.1:n.790T>C
ENST00000687786.1:n.2102T>C
ENST00000688100.1:n.1587T>C
ENST00000688588.1:c.666T>C	ENSP00000510802.1:p.Cys222=
ENST00000688927.1:n.2877T>C
ENST00000689283.1:c.*329T>C	ENSP00000509050.1:n.*329T>C
ENST00000689477.1:c.*559T>C	ENSP00000508945.1:n.*559T>C
ENST00000689765.1:c.*169-10T>C	ENSP00000509625.1:n.*169-10T>C
ENST00000690512.1:c.*517T>C	ENSP00000509793.1:n.*517T>C
ENST00000692039.1:c.*464T>C	ENSP00000508821.1:n.*464T>C
ENST00000692336.1:c.690T>C	ENSP00000508540.1:p.Cys230=
ENST00000693133.1:n.1146T>C
ENST00000263578.10:c.666T>C MANE Select	ENSP00000263578.5:p.Cys222=
ENST00000263578.9:c.666T>C	ENSP00000263578.5:p.Cys222=
ENST00000525083.5:n.386T>C
ENST00000525770.5:c.*298T>C	ENSP00000434739.1:n.*298T>C
ENST00000527004.5:c.*10T>C	ENSP00000436374.1:n.*10T>C
ENST00000530642.1:n.1448T>C
ENST00000532101.5:n.889T>C
ENST00000532125.1:c.624T>C	ENSP00000434178.1:p.Cys208=
ENST00000533395.5:n.399T>C
ENST00000533839.5:n.238-433T>C
ENST00000534011.5:n.718T>C
ENST00000534315.5:n.978T>C
NM_017547.3:c.666T>C	NP_060017.1:p.Cys222=
NR_037647.1:n.612T>C
NR_037648.1:n.852T>C
XM_006718879.2:c.156T>C	XP_006718942.1:p.Cys52=
XM_006718880.2:c.33T>C	XP_006718943.1:p.Cys11=
XM_006718881.2:c.33T>C	XP_006718944.1:p.Cys11=
XM_011542895.1:c.156T>C	XP_011541197.1:p.Cys52=
XM_011542896.1:c.156T>C	XP_011541198.1:p.Cys52=
XM_006718879.3:c.156T>C	XP_006718942.1:p.Cys52=
XM_006718881.3:c.33T>C	XP_006718944.1:p.Cys11=
XM_011542895.2:c.156T>C	XP_011541197.1:p.Cys52=
XM_011542896.2:c.156T>C	XP_011541198.1:p.Cys52=
XM_017018000.2:c.666T>C	XP_016873489.1:p.Cys222=
XM_017018001.1:c.156T>C	XP_016873490.1:p.Cys52=
XM_017018002.1:c.156T>C	XP_016873491.1:p.Cys52=
XM_017018003.2:c.33T>C	XP_016873492.1:p.Cys11=
XM_017018004.1:c.33T>C	XP_016873493.1:p.Cys11=
XM_017018005.1:c.33T>C	XP_016873494.1:p.Cys11=
XM_017018006.2:c.33T>C	XP_016873495.1:p.Cys11=
NM_017547.4:c.666T>C MANE Select	NP_060017.1:p.Cys222=
NR_037647.2:n.498T>C
NR_037648.2:n.843T>C