Canonical Allele Identifier: CA2007079552

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274991_126274993delinsAAC , CM000673.2:g.126274991_126274993delinsAAC	GRCh38
NC_000011.9:g.126144886_126144888delinsAAC , CM000673.1:g.126144886_126144888delinsAAC	GRCh37
NC_000011.8:g.125650096_125650098delinsAAC	NCBI36
NG_028029.1:g.10952_10954delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.779_781delinsAAC
ENST00000532101.6:n.734-336_734-334delinsAAC
ENST00000532125.2:c.598_600delinsAAC	ENSP00000434178.2:p.Asn200=
ENST00000533839.6:c.86-803_86-801delinsAAC	ENSP00000509952.1:n.86-803_86-801delinsAAC
ENST00000534011.6:n.893_895delinsAAC
ENST00000685484.1:c.601_603delinsAAC	ENSP00000510622.1:p.Asn201=
ENST00000685601.1:c.601_603delinsAAC	ENSP00000510603.1:p.Asn201=
ENST00000685765.1:c.601_603delinsAAC	ENSP00000509991.1:p.Asn201=
ENST00000685844.1:c.*169-336_*169-334delinsAAC	ENSP00000509820.1:n.*169-336_*169-334delinsAAC
ENST00000685857.1:n.1035_1037delinsAAC
ENST00000686242.1:c.400_402delinsAAC	ENSP00000508950.1:n.400_402delinsAAC
ENST00000686888.1:c.*168_*170delinsAAC	ENSP00000509619.1:n.*168_*170delinsAAC
ENST00000687699.1:c.725_727delinsAAC	ENSP00000508878.1:n.725_727delinsAAC
ENST00000687786.1:n.2068-336_2068-334delinsAAC
ENST00000688100.1:n.1522_1524delinsAAC
ENST00000688588.1:c.601_603delinsAAC	ENSP00000510802.1:p.Asn201=
ENST00000688927.1:n.2507_2509delinsAAC
ENST00000689283.1:c.*264_*266delinsAAC	ENSP00000509050.1:n.*264_*266delinsAAC
ENST00000689477.1:c.*494_*496delinsAAC	ENSP00000508945.1:n.*494_*496delinsAAC
ENST00000689765.1:c.*169-380_*169-378delinsAAC	ENSP00000509625.1:n.*169-380_*169-378delinsAAC
ENST00000690512.1:c.*452_*454delinsAAC	ENSP00000509793.1:n.*452_*454delinsAAC
ENST00000692039.1:c.*399_*401delinsAAC	ENSP00000508821.1:n.*399_*401delinsAAC
ENST00000692336.1:c.625_627delinsAAC	ENSP00000508540.1:p.Asn209=
ENST00000693133.1:n.776_778delinsAAC
ENST00000263578.10:c.601_603delinsAAC MANE Select	ENSP00000263578.5:p.Asn201=
ENST00000263578.9:c.601_603delinsAAC	ENSP00000263578.5:p.Asn201=
ENST00000524751.5:n.537_539delinsAAC
ENST00000525083.5:n.352-336_352-334delinsAAC
ENST00000525770.5:c.*233_*235delinsAAC	ENSP00000434739.1:n.*233_*235delinsAAC
ENST00000526366.5:n.532_534delinsAAC
ENST00000527004.5:c.534-336_534-334delinsAAC	ENSP00000436374.1:n.534-336_534-334delinsAAC
ENST00000527875.1:n.431_433delinsAAC
ENST00000530642.1:n.1078_1080delinsAAC
ENST00000532101.5:n.824_826delinsAAC
ENST00000532125.1:c.559_561delinsAAC	ENSP00000434178.1:p.Asn187=
ENST00000533395.5:n.365-336_365-334delinsAAC
ENST00000533839.5:n.238-803_238-801delinsAAC
ENST00000534011.5:n.653_655delinsAAC
ENST00000534315.5:n.944-336_944-334delinsAAC
NM_017547.3:c.601_603delinsAAC	NP_060017.1:p.Asn201=
NR_037647.1:n.547_549delinsAAC
NR_037648.1:n.787_789delinsAAC
XM_006718879.2:c.91_93delinsAAC	XP_006718942.1:p.Asn31=
XM_006718880.2:c.-2-336_-2-334delinsAAC	XP_006718943.1:n.-2-336_-2-334delinsAAC
XM_006718881.2:c.-2-336_-2-334delinsAAC	XP_006718944.1:n.-2-336_-2-334delinsAAC
XM_011542895.1:c.91_93delinsAAC	XP_011541197.1:p.Asn31=
XM_011542896.1:c.91_93delinsAAC	XP_011541198.1:p.Asn31=
XM_006718879.3:c.91_93delinsAAC	XP_006718942.1:p.Asn31=
XM_006718881.3:c.-2-336_-2-334delinsAAC	XP_006718944.1:n.-2-336_-2-334delinsAAC
XM_011542895.2:c.91_93delinsAAC	XP_011541197.1:p.Asn31=
XM_011542896.2:c.91_93delinsAAC	XP_011541198.1:p.Asn31=
XM_017018000.2:c.601_603delinsAAC	XP_016873489.1:p.Asn201=
XM_017018001.1:c.91_93delinsAAC	XP_016873490.1:p.Asn31=
XM_017018002.1:c.91_93delinsAAC	XP_016873491.1:p.Asn31=
XM_017018003.2:c.-2-336_-2-334delinsAAC	XP_016873492.1:n.-2-336_-2-334delinsAAC
XM_017018004.1:c.-2-336_-2-334delinsAAC	XP_016873493.1:n.-2-336_-2-334delinsAAC
XM_017018005.1:c.-2-336_-2-334delinsAAC	XP_016873494.1:n.-2-336_-2-334delinsAAC
XM_017018006.2:c.-2-336_-2-334delinsAAC	XP_016873495.1:n.-2-336_-2-334delinsAAC
NM_017547.4:c.601_603delinsAAC MANE Select	NP_060017.1:p.Asn201=
NR_037647.2:n.433_435delinsAAC
NR_037648.2:n.778_780delinsAAC