Canonical Allele Identifier: CA2575022762

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275252-TGGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275256_126275258del , CM000673.2:g.126275256_126275258del	GRCh38
NC_000011.9:g.126145151_126145153del , CM000673.1:g.126145151_126145153del	GRCh37
NC_000011.8:g.125650361_125650363del	NCBI36
NG_028029.1:g.11217_11219del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1044_1046del
ENST00000532101.6:n.734-71_734-69del
ENST00000532125.2:c.629-71_629-69del	ENSP00000434178.2:n.629-71_629-69del
ENST00000533839.6:c.86-538_86-536del	ENSP00000509952.1:n.86-538_86-536del
ENST00000534011.6:n.924-71_924-69del
ENST00000685484.1:c.632-71_632-69del	ENSP00000510622.1:n.632-71_632-69del
ENST00000685601.1:c.632-71_632-69del	ENSP00000510603.1:n.632-71_632-69del
ENST00000685765.1:c.632-71_632-69del	ENSP00000509991.1:n.632-71_632-69del
ENST00000685844.1:c.*169-71_*169-69del	ENSP00000509820.1:n.*169-71_*169-69del
ENST00000685857.1:n.1300_1302del
ENST00000686242.1:c.431-71_431-69del	ENSP00000508950.1:n.431-71_431-69del
ENST00000686888.1:c.*199-71_*199-69del	ENSP00000509619.1:n.*199-71_*199-69del
ENST00000687699.1:c.756-71_756-69del	ENSP00000508878.1:n.756-71_756-69del
ENST00000687786.1:n.2068-71_2068-69del
ENST00000688100.1:n.1553-71_1553-69del
ENST00000688588.1:c.632-71_632-69del	ENSP00000510802.1:n.632-71_632-69del
ENST00000688927.1:n.2772_2774del
ENST00000689283.1:c.*295-71_*295-69del	ENSP00000509050.1:n.*295-71_*295-69del
ENST00000689477.1:c.*525-71_*525-69del	ENSP00000508945.1:n.*525-71_*525-69del
ENST00000689765.1:c.*169-115_*169-113del	ENSP00000509625.1:n.*169-115_*169-113del
ENST00000690512.1:c.*483-71_*483-69del	ENSP00000509793.1:n.*483-71_*483-69del
ENST00000692039.1:c.*430-71_*430-69del	ENSP00000508821.1:n.*430-71_*430-69del
ENST00000692336.1:c.656-71_656-69del	ENSP00000508540.1:n.656-71_656-69del
ENST00000693133.1:n.1041_1043del
ENST00000263578.10:c.632-71_632-69del MANE Select	ENSP00000263578.5:n.632-71_632-69del
ENST00000263578.9:c.632-71_632-69del	ENSP00000263578.5:n.632-71_632-69del
ENST00000524751.5:n.802_804del
ENST00000525083.5:n.352-71_352-69del
ENST00000525770.5:c.*264-71_*264-69del	ENSP00000434739.1:n.*264-71_*264-69del
ENST00000527004.5:c.534-71_534-69del	ENSP00000436374.1:n.534-71_534-69del
ENST00000530642.1:n.1343_1345del
ENST00000532101.5:n.855-71_855-69del
ENST00000532125.1:c.590-71_590-69del	ENSP00000434178.1:n.590-71_590-69del
ENST00000533395.5:n.365-71_365-69del
ENST00000533839.5:n.238-538_238-536del
ENST00000534011.5:n.684-71_684-69del
ENST00000534315.5:n.944-71_944-69del
NM_017547.3:c.632-71_632-69del	NP_060017.1:n.632-71_632-69del
NR_037647.1:n.578-71_578-69del
NR_037648.1:n.818-71_818-69del
XM_006718879.2:c.122-71_122-69del	XP_006718942.1:n.122-71_122-69del
XM_006718880.2:c.-2-71_-2-69del	XP_006718943.1:n.-2-71_-2-69del
XM_006718881.2:c.-2-71_-2-69del	XP_006718944.1:n.-2-71_-2-69del
XM_011542895.1:c.122-71_122-69del	XP_011541197.1:n.122-71_122-69del
XM_011542896.1:c.122-71_122-69del	XP_011541198.1:n.122-71_122-69del
XM_006718879.3:c.122-71_122-69del	XP_006718942.1:n.122-71_122-69del
XM_006718881.3:c.-2-71_-2-69del	XP_006718944.1:n.-2-71_-2-69del
XM_011542895.2:c.122-71_122-69del	XP_011541197.1:n.122-71_122-69del
XM_011542896.2:c.122-71_122-69del	XP_011541198.1:n.122-71_122-69del
XM_017018000.2:c.632-71_632-69del	XP_016873489.1:n.632-71_632-69del
XM_017018001.1:c.122-71_122-69del	XP_016873490.1:n.122-71_122-69del
XM_017018002.1:c.122-71_122-69del	XP_016873491.1:n.122-71_122-69del
XM_017018003.2:c.-2-71_-2-69del	XP_016873492.1:n.-2-71_-2-69del
XM_017018004.1:c.-2-71_-2-69del	XP_016873493.1:n.-2-71_-2-69del
XM_017018005.1:c.-2-71_-2-69del	XP_016873494.1:n.-2-71_-2-69del
XM_017018006.2:c.-2-71_-2-69del	XP_016873495.1:n.-2-71_-2-69del
NM_017547.4:c.632-71_632-69del MANE Select	NP_060017.1:n.632-71_632-69del
NR_037647.2:n.464-71_464-69del
NR_037648.2:n.809-71_809-69del