Canonical Allele Identifier: CA2616722450

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275319-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275320del , CM000673.2:g.126275320del	GRCh38
NC_000011.9:g.126145215del , CM000673.1:g.126145215del	GRCh37
NC_000011.8:g.125650425del	NCBI36
NG_028029.1:g.11281del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1108del
ENST00000532101.6:n.734-7del
ENST00000532125.2:c.629-7del	ENSP00000434178.2:n.629-7del
ENST00000533839.6:c.86-474del	ENSP00000509952.1:n.86-474del
ENST00000534011.6:n.924-7del
ENST00000685484.1:c.632-7del	ENSP00000510622.1:n.632-7del
ENST00000685601.1:c.632-7del	ENSP00000510603.1:n.632-7del
ENST00000685765.1:c.632-7del	ENSP00000509991.1:n.632-7del
ENST00000685844.1:c.*169-7del	ENSP00000509820.1:n.*169-7del
ENST00000685857.1:n.1364del
ENST00000686242.1:c.431-7del	ENSP00000508950.1:n.431-7del
ENST00000686888.1:c.*199-7del	ENSP00000509619.1:n.*199-7del
ENST00000687699.1:c.756-7del	ENSP00000508878.1:n.756-7del
ENST00000687786.1:n.2068-7del
ENST00000688100.1:n.1553-7del
ENST00000688588.1:c.632-7del	ENSP00000510802.1:n.632-7del
ENST00000688927.1:n.2836del
ENST00000689283.1:c.*295-7del	ENSP00000509050.1:n.*295-7del
ENST00000689477.1:c.*525-7del	ENSP00000508945.1:n.*525-7del
ENST00000689765.1:c.*169-51del	ENSP00000509625.1:n.*169-51del
ENST00000690512.1:c.*483-7del	ENSP00000509793.1:n.*483-7del
ENST00000692039.1:c.*430-7del	ENSP00000508821.1:n.*430-7del
ENST00000692336.1:c.656-7del	ENSP00000508540.1:n.656-7del
ENST00000693133.1:n.1105del
ENST00000263578.10:c.632-7del MANE Select	ENSP00000263578.5:n.632-7del
ENST00000263578.9:c.632-7del	ENSP00000263578.5:n.632-7del
ENST00000524751.5:n.866del
ENST00000525083.5:n.352-7del
ENST00000525770.5:c.*264-7del	ENSP00000434739.1:n.*264-7del
ENST00000527004.5:c.534-7del	ENSP00000436374.1:n.534-7del
ENST00000530642.1:n.1407del
ENST00000532101.5:n.855-7del
ENST00000532125.1:c.590-7del	ENSP00000434178.1:n.590-7del
ENST00000533395.5:n.365-7del
ENST00000533839.5:n.238-474del
ENST00000534011.5:n.684-7del
ENST00000534315.5:n.944-7del
NM_017547.3:c.632-7del	NP_060017.1:n.632-7del
NR_037647.1:n.578-7del
NR_037648.1:n.818-7del
XM_006718879.2:c.122-7del	XP_006718942.1:n.122-7del
XM_006718880.2:c.-2-7del	XP_006718943.1:n.-2-7del
XM_006718881.2:c.-2-7del	XP_006718944.1:n.-2-7del
XM_011542895.1:c.122-7del	XP_011541197.1:n.122-7del
XM_011542896.1:c.122-7del	XP_011541198.1:n.122-7del
XM_006718879.3:c.122-7del	XP_006718942.1:n.122-7del
XM_006718881.3:c.-2-7del	XP_006718944.1:n.-2-7del
XM_011542895.2:c.122-7del	XP_011541197.1:n.122-7del
XM_011542896.2:c.122-7del	XP_011541198.1:n.122-7del
XM_017018000.2:c.632-7del	XP_016873489.1:n.632-7del
XM_017018001.1:c.122-7del	XP_016873490.1:n.122-7del
XM_017018002.1:c.122-7del	XP_016873491.1:n.122-7del
XM_017018003.2:c.-2-7del	XP_016873492.1:n.-2-7del
XM_017018004.1:c.-2-7del	XP_016873493.1:n.-2-7del
XM_017018005.1:c.-2-7del	XP_016873494.1:n.-2-7del
XM_017018006.2:c.-2-7del	XP_016873495.1:n.-2-7del
NM_017547.4:c.632-7del MANE Select	NP_060017.1:n.632-7del
NR_037647.2:n.464-7del
NR_037648.2:n.809-7del