Canonical Allele Identifier: CA2007079543

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274974_126274975delinsAC , CM000673.2:g.126274974_126274975delinsAC	GRCh38
NC_000011.9:g.126144869_126144870delinsAC , CM000673.1:g.126144869_126144870delinsAC	GRCh37
NC_000011.8:g.125650079_125650080delinsAC	NCBI36
NG_028029.1:g.10935_10936delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.762_763delinsAC
ENST00000532101.6:n.734-353_734-352delinsAC
ENST00000532125.2:c.581_582delinsAC	ENSP00000434178.2:p.Asn194=
ENST00000533839.6:c.86-820_86-819delinsAC	ENSP00000509952.1:n.86-820_86-819delinsAC
ENST00000534011.6:n.876_877delinsAC
ENST00000685484.1:c.584_585delinsAC	ENSP00000510622.1:p.Asn195=
ENST00000685601.1:c.584_585delinsAC	ENSP00000510603.1:p.Asn195=
ENST00000685765.1:c.584_585delinsAC	ENSP00000509991.1:p.Asn195=
ENST00000685844.1:c.*169-353_*169-352delinsAC	ENSP00000509820.1:n.*169-353_*169-352delinsAC
ENST00000685857.1:n.1018_1019delinsAC
ENST00000686242.1:c.383_384delinsAC	ENSP00000508950.1:n.383_384delinsAC
ENST00000686888.1:c.*151_*152delinsAC	ENSP00000509619.1:n.*151_*152delinsAC
ENST00000687699.1:c.708_709delinsAC	ENSP00000508878.1:n.708_709delinsAC
ENST00000687786.1:n.2068-353_2068-352delinsAC
ENST00000688100.1:n.1505_1506delinsAC
ENST00000688588.1:c.584_585delinsAC	ENSP00000510802.1:p.Asn195=
ENST00000688927.1:n.2490_2491delinsAC
ENST00000689283.1:c.*247_*248delinsAC	ENSP00000509050.1:n.*247_*248delinsAC
ENST00000689477.1:c.*477_*478delinsAC	ENSP00000508945.1:n.*477_*478delinsAC
ENST00000689765.1:c.*169-397_*169-396delinsAC	ENSP00000509625.1:n.*169-397_*169-396delinsAC
ENST00000690512.1:c.*435_*436delinsAC	ENSP00000509793.1:n.*435_*436delinsAC
ENST00000692039.1:c.*382_*383delinsAC	ENSP00000508821.1:n.*382_*383delinsAC
ENST00000692336.1:c.608_609delinsAC	ENSP00000508540.1:p.Asn203=
ENST00000693133.1:n.759_760delinsAC
ENST00000263578.10:c.584_585delinsAC MANE Select	ENSP00000263578.5:p.Asn195=
ENST00000263578.9:c.584_585delinsAC	ENSP00000263578.5:p.Asn195=
ENST00000524751.5:n.520_521delinsAC
ENST00000525083.5:n.352-353_352-352delinsAC
ENST00000525770.5:c.*216_*217delinsAC	ENSP00000434739.1:n.*216_*217delinsAC
ENST00000526366.5:n.515_516delinsAC
ENST00000527004.5:c.534-353_534-352delinsAC	ENSP00000436374.1:n.534-353_534-352delinsAC
ENST00000527875.1:n.414_415delinsAC
ENST00000530642.1:n.1061_1062delinsAC
ENST00000532101.5:n.807_808delinsAC
ENST00000532125.1:c.542_543delinsAC	ENSP00000434178.1:p.Asn181=
ENST00000533395.5:n.365-353_365-352delinsAC
ENST00000533839.5:n.238-820_238-819delinsAC
ENST00000534011.5:n.636_637delinsAC
ENST00000534315.5:n.944-353_944-352delinsAC
NM_017547.3:c.584_585delinsAC	NP_060017.1:p.Asn195=
NR_037647.1:n.530_531delinsAC
NR_037648.1:n.770_771delinsAC
XM_006718879.2:c.74_75delinsAC	XP_006718942.1:p.Asn25=
XM_006718880.2:c.-2-353_-2-352delinsAC	XP_006718943.1:n.-2-353_-2-352delinsAC
XM_006718881.2:c.-2-353_-2-352delinsAC	XP_006718944.1:n.-2-353_-2-352delinsAC
XM_011542895.1:c.74_75delinsAC	XP_011541197.1:p.Asn25=
XM_011542896.1:c.74_75delinsAC	XP_011541198.1:p.Asn25=
XM_006718879.3:c.74_75delinsAC	XP_006718942.1:p.Asn25=
XM_006718881.3:c.-2-353_-2-352delinsAC	XP_006718944.1:n.-2-353_-2-352delinsAC
XM_011542895.2:c.74_75delinsAC	XP_011541197.1:p.Asn25=
XM_011542896.2:c.74_75delinsAC	XP_011541198.1:p.Asn25=
XM_017018000.2:c.584_585delinsAC	XP_016873489.1:p.Asn195=
XM_017018001.1:c.74_75delinsAC	XP_016873490.1:p.Asn25=
XM_017018002.1:c.74_75delinsAC	XP_016873491.1:p.Asn25=
XM_017018003.2:c.-2-353_-2-352delinsAC	XP_016873492.1:n.-2-353_-2-352delinsAC
XM_017018004.1:c.-2-353_-2-352delinsAC	XP_016873493.1:n.-2-353_-2-352delinsAC
XM_017018005.1:c.-2-353_-2-352delinsAC	XP_016873494.1:n.-2-353_-2-352delinsAC
XM_017018006.2:c.-2-353_-2-352delinsAC	XP_016873495.1:n.-2-353_-2-352delinsAC
NM_017547.4:c.584_585delinsAC MANE Select	NP_060017.1:p.Asn195=
NR_037647.2:n.416_417delinsAC
NR_037648.2:n.761_762delinsAC