Canonical Allele Identifier: CA383230180

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145270T>C (hg19) ; chr11:g.126275375T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275375T>C , CM000673.2:g.126275375T>C	GRCh38
NC_000011.9:g.126145270T>C , CM000673.1:g.126145270T>C	GRCh37
NC_000011.8:g.125650480T>C	NCBI36
NG_028029.1:g.11336T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1163T>C
ENST00000532101.6:n.782T>C
ENST00000532125.2:c.677T>C	ENSP00000434178.2:p.Leu226Pro
ENST00000533839.6:c.86-419T>C	ENSP00000509952.1:n.86-419T>C
ENST00000534011.6:n.972T>C
ENST00000685484.1:c.680T>C	ENSP00000510622.1:p.Leu227Pro
ENST00000685601.1:c.680T>C	ENSP00000510603.1:p.Leu227Pro
ENST00000685765.1:c.680T>C	ENSP00000509991.1:p.Leu227Pro
ENST00000685844.1:c.*217T>C	ENSP00000509820.1:n.*217T>C
ENST00000685857.1:n.1419T>C
ENST00000686242.1:c.479T>C	ENSP00000508950.1:n.479T>C
ENST00000686888.1:c.*247T>C	ENSP00000509619.1:n.*247T>C
ENST00000687699.1:c.804T>C	ENSP00000508878.1:n.804T>C
ENST00000687786.1:n.2116T>C
ENST00000688100.1:n.1601T>C
ENST00000688588.1:c.680T>C	ENSP00000510802.1:p.Leu227Pro
ENST00000688927.1:n.2891T>C
ENST00000689283.1:c.*343T>C	ENSP00000509050.1:n.*343T>C
ENST00000689477.1:c.*573T>C	ENSP00000508945.1:n.*573T>C
ENST00000689765.1:c.*173T>C	ENSP00000509625.1:n.*173T>C
ENST00000690512.1:c.*531T>C	ENSP00000509793.1:n.*531T>C
ENST00000692039.1:c.*478T>C	ENSP00000508821.1:n.*478T>C
ENST00000692336.1:c.704T>C	ENSP00000508540.1:p.Leu235Pro
ENST00000693133.1:n.1160T>C
ENST00000263578.10:c.680T>C MANE Select	ENSP00000263578.5:p.Leu227Pro
ENST00000263578.9:c.680T>C	ENSP00000263578.5:p.Leu227Pro
ENST00000525083.5:n.400T>C
ENST00000525770.5:c.*312T>C	ENSP00000434739.1:n.*312T>C
ENST00000527004.5:c.*24T>C	ENSP00000436374.1:n.*24T>C
ENST00000530642.1:n.1462T>C
ENST00000532101.5:n.903T>C
ENST00000532125.1:c.638T>C	ENSP00000434178.1:p.Leu213Pro
ENST00000533395.5:n.413T>C
ENST00000533839.5:n.238-419T>C
ENST00000534011.5:n.732T>C
ENST00000534315.5:n.992T>C
NM_017547.3:c.680T>C	NP_060017.1:p.Leu227Pro
NR_037647.1:n.626T>C
NR_037648.1:n.866T>C
XM_006718879.2:c.170T>C	XP_006718942.1:p.Leu57Pro
XM_006718880.2:c.47T>C	XP_006718943.1:p.Leu16Pro
XM_006718881.2:c.47T>C	XP_006718944.1:p.Leu16Pro
XM_011542895.1:c.170T>C	XP_011541197.1:p.Leu57Pro
XM_011542896.1:c.170T>C	XP_011541198.1:p.Leu57Pro
XM_006718879.3:c.170T>C	XP_006718942.1:p.Leu57Pro
XM_006718881.3:c.47T>C	XP_006718944.1:p.Leu16Pro
XM_011542895.2:c.170T>C	XP_011541197.1:p.Leu57Pro
XM_011542896.2:c.170T>C	XP_011541198.1:p.Leu57Pro
XM_017018000.2:c.680T>C	XP_016873489.1:p.Leu227Pro
XM_017018001.1:c.170T>C	XP_016873490.1:p.Leu57Pro
XM_017018002.1:c.170T>C	XP_016873491.1:p.Leu57Pro
XM_017018003.2:c.47T>C	XP_016873492.1:p.Leu16Pro
XM_017018004.1:c.47T>C	XP_016873493.1:p.Leu16Pro
XM_017018005.1:c.47T>C	XP_016873494.1:p.Leu16Pro
XM_017018006.2:c.47T>C	XP_016873495.1:p.Leu16Pro
NM_017547.4:c.680T>C MANE Select	NP_060017.1:p.Leu227Pro
NR_037647.2:n.512T>C
NR_037648.2:n.857T>C