Canonical Allele Identifier: CA2007079653

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1951097082

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275251_126275254del , CM000673.2:g.126275251_126275254del	GRCh38
NC_000011.9:g.126145146_126145149del , CM000673.1:g.126145146_126145149del	GRCh37
NC_000011.8:g.125650356_125650359del	NCBI36
NG_028029.1:g.11212_11215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1039_1042del
ENST00000532101.6:n.734-76_734-73del
ENST00000532125.2:c.629-76_629-73del	ENSP00000434178.2:n.629-76_629-73del
ENST00000533839.6:c.86-543_86-540del	ENSP00000509952.1:n.86-543_86-540del
ENST00000534011.6:n.924-76_924-73del
ENST00000685484.1:c.632-76_632-73del	ENSP00000510622.1:n.632-76_632-73del
ENST00000685601.1:c.632-76_632-73del	ENSP00000510603.1:n.632-76_632-73del
ENST00000685765.1:c.632-76_632-73del	ENSP00000509991.1:n.632-76_632-73del
ENST00000685844.1:c.*169-76_*169-73del	ENSP00000509820.1:n.*169-76_*169-73del
ENST00000685857.1:n.1295_1298del
ENST00000686242.1:c.431-76_431-73del	ENSP00000508950.1:n.431-76_431-73del
ENST00000686888.1:c.*199-76_*199-73del	ENSP00000509619.1:n.*199-76_*199-73del
ENST00000687699.1:c.756-76_756-73del	ENSP00000508878.1:n.756-76_756-73del
ENST00000687786.1:n.2068-76_2068-73del
ENST00000688100.1:n.1553-76_1553-73del
ENST00000688588.1:c.632-76_632-73del	ENSP00000510802.1:n.632-76_632-73del
ENST00000688927.1:n.2767_2770del
ENST00000689283.1:c.*295-76_*295-73del	ENSP00000509050.1:n.*295-76_*295-73del
ENST00000689477.1:c.*525-76_*525-73del	ENSP00000508945.1:n.*525-76_*525-73del
ENST00000689765.1:c.*169-120_*169-117del	ENSP00000509625.1:n.*169-120_*169-117del
ENST00000690512.1:c.*483-76_*483-73del	ENSP00000509793.1:n.*483-76_*483-73del
ENST00000692039.1:c.*430-76_*430-73del	ENSP00000508821.1:n.*430-76_*430-73del
ENST00000692336.1:c.656-76_656-73del	ENSP00000508540.1:n.656-76_656-73del
ENST00000693133.1:n.1036_1039del
ENST00000263578.10:c.632-76_632-73del MANE Select	ENSP00000263578.5:n.632-76_632-73del
ENST00000263578.9:c.632-76_632-73del	ENSP00000263578.5:n.632-76_632-73del
ENST00000524751.5:n.797_800del
ENST00000525083.5:n.352-76_352-73del
ENST00000525770.5:c.*264-76_*264-73del	ENSP00000434739.1:n.*264-76_*264-73del
ENST00000527004.5:c.534-76_534-73del	ENSP00000436374.1:n.534-76_534-73del
ENST00000530642.1:n.1338_1341del
ENST00000532101.5:n.855-76_855-73del
ENST00000532125.1:c.590-76_590-73del	ENSP00000434178.1:n.590-76_590-73del
ENST00000533395.5:n.365-76_365-73del
ENST00000533839.5:n.238-543_238-540del
ENST00000534011.5:n.684-76_684-73del
ENST00000534315.5:n.944-76_944-73del
NM_017547.3:c.632-76_632-73del	NP_060017.1:n.632-76_632-73del
NR_037647.1:n.578-76_578-73del
NR_037648.1:n.818-76_818-73del
XM_006718879.2:c.122-76_122-73del	XP_006718942.1:n.122-76_122-73del
XM_006718880.2:c.-2-76_-2-73del	XP_006718943.1:n.-2-76_-2-73del
XM_006718881.2:c.-2-76_-2-73del	XP_006718944.1:n.-2-76_-2-73del
XM_011542895.1:c.122-76_122-73del	XP_011541197.1:n.122-76_122-73del
XM_011542896.1:c.122-76_122-73del	XP_011541198.1:n.122-76_122-73del
XM_006718879.3:c.122-76_122-73del	XP_006718942.1:n.122-76_122-73del
XM_006718881.3:c.-2-76_-2-73del	XP_006718944.1:n.-2-76_-2-73del
XM_011542895.2:c.122-76_122-73del	XP_011541197.1:n.122-76_122-73del
XM_011542896.2:c.122-76_122-73del	XP_011541198.1:n.122-76_122-73del
XM_017018000.2:c.632-76_632-73del	XP_016873489.1:n.632-76_632-73del
XM_017018001.1:c.122-76_122-73del	XP_016873490.1:n.122-76_122-73del
XM_017018002.1:c.122-76_122-73del	XP_016873491.1:n.122-76_122-73del
XM_017018003.2:c.-2-76_-2-73del	XP_016873492.1:n.-2-76_-2-73del
XM_017018004.1:c.-2-76_-2-73del	XP_016873493.1:n.-2-76_-2-73del
XM_017018005.1:c.-2-76_-2-73del	XP_016873494.1:n.-2-76_-2-73del
XM_017018006.2:c.-2-76_-2-73del	XP_016873495.1:n.-2-76_-2-73del
NM_017547.4:c.632-76_632-73del MANE Select	NP_060017.1:n.632-76_632-73del
NR_037647.2:n.464-76_464-73del
NR_037648.2:n.809-76_809-73del