Canonical Allele Identifier: CA383230216

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145291T>C (hg19) ; chr11:g.126275396T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275396T>C , CM000673.2:g.126275396T>C	GRCh38
NC_000011.9:g.126145291T>C , CM000673.1:g.126145291T>C	GRCh37
NC_000011.8:g.125650501T>C	NCBI36
NG_028029.1:g.11357T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1184T>C
ENST00000532101.6:n.803T>C
ENST00000532125.2:c.698T>C	ENSP00000434178.2:p.Leu233Ser
ENST00000533839.6:c.86-398T>C	ENSP00000509952.1:n.86-398T>C
ENST00000534011.6:n.993T>C
ENST00000685484.1:c.701T>C	ENSP00000510622.1:p.Leu234Ser
ENST00000685601.1:c.701T>C	ENSP00000510603.1:p.Leu234Ser
ENST00000685765.1:c.701T>C	ENSP00000509991.1:p.Leu234Ser
ENST00000685844.1:c.*238T>C	ENSP00000509820.1:n.*238T>C
ENST00000685857.1:n.1440T>C
ENST00000686242.1:c.500T>C	ENSP00000508950.1:n.500T>C
ENST00000686888.1:c.*268T>C	ENSP00000509619.1:n.*268T>C
ENST00000687699.1:c.825T>C	ENSP00000508878.1:n.825T>C
ENST00000687786.1:n.2137T>C
ENST00000688100.1:n.1622T>C
ENST00000688588.1:c.701T>C	ENSP00000510802.1:p.Leu234Ser
ENST00000688927.1:n.2912T>C
ENST00000689283.1:c.*364T>C	ENSP00000509050.1:n.*364T>C
ENST00000689477.1:c.*594T>C	ENSP00000508945.1:n.*594T>C
ENST00000689765.1:c.*194T>C	ENSP00000509625.1:n.*194T>C
ENST00000690512.1:c.*552T>C	ENSP00000509793.1:n.*552T>C
ENST00000692039.1:c.*499T>C	ENSP00000508821.1:n.*499T>C
ENST00000692336.1:c.725T>C	ENSP00000508540.1:p.Leu242Ser
ENST00000693133.1:n.1181T>C
ENST00000263578.10:c.701T>C MANE Select	ENSP00000263578.5:p.Leu234Ser
ENST00000263578.9:c.701T>C	ENSP00000263578.5:p.Leu234Ser
ENST00000525083.5:n.421T>C
ENST00000525770.5:c.*333T>C	ENSP00000434739.1:n.*333T>C
ENST00000527004.5:c.*45T>C	ENSP00000436374.1:n.*45T>C
ENST00000530642.1:n.1483T>C
ENST00000532101.5:n.924T>C
ENST00000532125.1:c.659T>C	ENSP00000434178.1:p.Leu220Ser
ENST00000533395.5:n.434T>C
ENST00000533839.5:n.238-398T>C
ENST00000534011.5:n.753T>C
ENST00000534315.5:n.1013T>C
NM_017547.3:c.701T>C	NP_060017.1:p.Leu234Ser
NR_037647.1:n.647T>C
NR_037648.1:n.887T>C
XM_006718879.2:c.191T>C	XP_006718942.1:p.Leu64Ser
XM_006718880.2:c.68T>C	XP_006718943.1:p.Leu23Ser
XM_006718881.2:c.68T>C	XP_006718944.1:p.Leu23Ser
XM_011542895.1:c.191T>C	XP_011541197.1:p.Leu64Ser
XM_011542896.1:c.191T>C	XP_011541198.1:p.Leu64Ser
XM_006718879.3:c.191T>C	XP_006718942.1:p.Leu64Ser
XM_006718881.3:c.68T>C	XP_006718944.1:p.Leu23Ser
XM_011542895.2:c.191T>C	XP_011541197.1:p.Leu64Ser
XM_011542896.2:c.191T>C	XP_011541198.1:p.Leu64Ser
XM_017018000.2:c.701T>C	XP_016873489.1:p.Leu234Ser
XM_017018001.1:c.191T>C	XP_016873490.1:p.Leu64Ser
XM_017018002.1:c.191T>C	XP_016873491.1:p.Leu64Ser
XM_017018003.2:c.68T>C	XP_016873492.1:p.Leu23Ser
XM_017018004.1:c.68T>C	XP_016873493.1:p.Leu23Ser
XM_017018005.1:c.68T>C	XP_016873494.1:p.Leu23Ser
XM_017018006.2:c.68T>C	XP_016873495.1:p.Leu23Ser
NM_017547.4:c.701T>C MANE Select	NP_060017.1:p.Leu234Ser
NR_037647.2:n.533T>C
NR_037648.2:n.878T>C