Canonical Allele Identifier: CA383230297

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275793G>C , CM000673.2:g.126275793G>C	GRCh38
NC_000011.9:g.126145688G>C , CM000673.1:g.126145688G>C	GRCh37
NC_000011.8:g.125650898G>C	NCBI36
NG_028029.1:g.11754G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_017547.4:c.734-1G>C MANE Select	NP_060017.1:n.734-1G>C
ENST00000263578.10:c.734-1G>C MANE Select	ENSP00000263578.5:n.734-1G>C
NM_017547.3:c.734-1G>C	NP_060017.1:n.734-1G>C
NR_037647.1:n.680-1G>C
NR_037647.2:n.566-1G>C
NR_037648.1:n.920-1G>C
NR_037648.2:n.911-1G>C
ENST00000263578.9:c.734-1G>C	ENSP00000263578.5:n.734-1G>C
ENST00000525083.5:n.454-1G>C
ENST00000525083.6:n.1217-1G>C
ENST00000525770.5:c.*366-1G>C	ENSP00000434739.1:n.*366-1G>C
ENST00000527004.5:c.*78-1G>C	ENSP00000436374.1:n.*78-1G>C
ENST00000530642.1:n.1880G>C
ENST00000532101.5:n.957-1G>C
ENST00000532101.6:n.836-1G>C
ENST00000532125.1:c.692-1G>C	ENSP00000434178.1:n.692-1G>C
ENST00000532125.2:c.731-1G>C	ENSP00000434178.2:n.731-1G>C
ENST00000533395.5:n.467-1G>C
ENST00000533839.5:n.238-1G>C
ENST00000533839.6:c.86-1G>C	ENSP00000509952.1:n.86-1G>C
ENST00000534011.5:n.786-1G>C
ENST00000534011.6:n.1026-1G>C
ENST00000534315.5:n.1046-1G>C
ENST00000685484.1:c.734-1G>C	ENSP00000510622.1:n.734-1G>C
ENST00000685601.1:c.734-1G>C	ENSP00000510603.1:n.734-1G>C
ENST00000685765.1:c.734-1G>C	ENSP00000509991.1:n.734-1G>C
ENST00000685844.1:c.*271-1G>C	ENSP00000509820.1:n.*271-1G>C
ENST00000685857.1:n.1837G>C
ENST00000686242.1:c.533-1G>C	ENSP00000508950.1:n.533-1G>C
ENST00000686888.1:c.*301-1G>C	ENSP00000509619.1:n.*301-1G>C
ENST00000687699.1:c.858-1G>C	ENSP00000508878.1:n.858-1G>C
ENST00000687786.1:n.2170-1G>C
ENST00000688100.1:n.1655-1G>C
ENST00000688588.1:c.734-1G>C	ENSP00000510802.1:n.734-1G>C
ENST00000688927.1:n.2945-1G>C
ENST00000689283.1:c.*397-1G>C	ENSP00000509050.1:n.*397-1G>C
ENST00000689477.1:c.*627-1G>C	ENSP00000508945.1:n.*627-1G>C
ENST00000689765.1:c.*227-1G>C	ENSP00000509625.1:n.*227-1G>C
ENST00000690512.1:c.*585-1G>C	ENSP00000509793.1:n.*585-1G>C
ENST00000692039.1:c.*532-1G>C	ENSP00000508821.1:n.*532-1G>C
ENST00000692336.1:c.758-1G>C	ENSP00000508540.1:n.758-1G>C
ENST00000693133.1:n.1578G>C
XM_006718879.2:c.224-1G>C	XP_006718942.1:n.224-1G>C
XM_006718879.3:c.224-1G>C	XP_006718942.1:n.224-1G>C
XM_006718880.2:c.101-1G>C	XP_006718943.1:n.101-1G>C
XM_006718881.2:c.101-1G>C	XP_006718944.1:n.101-1G>C
XM_006718881.3:c.101-1G>C	XP_006718944.1:n.101-1G>C
XM_011542895.1:c.224-1G>C	XP_011541197.1:n.224-1G>C
XM_011542895.2:c.224-1G>C	XP_011541197.1:n.224-1G>C
XM_011542896.1:c.224-1G>C	XP_011541198.1:n.224-1G>C
XM_011542896.2:c.224-1G>C	XP_011541198.1:n.224-1G>C
XM_017018000.2:c.734-1G>C	XP_016873489.1:n.734-1G>C
XM_017018001.1:c.224-1G>C	XP_016873490.1:n.224-1G>C
XM_017018002.1:c.224-1G>C	XP_016873491.1:n.224-1G>C
XM_017018003.2:c.101-1G>C	XP_016873492.1:n.101-1G>C
XM_017018004.1:c.101-1G>C	XP_016873493.1:n.101-1G>C
XM_017018005.1:c.101-1G>C	XP_016873494.1:n.101-1G>C
XM_017018006.2:c.101-1G>C	XP_016873495.1:n.101-1G>C