Canonical Allele Identifier: CA2616727076

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126271129-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271129G>A , CM000673.2:g.126271129G>A	GRCh38
NC_000011.9:g.126141024G>A , CM000673.1:g.126141024G>A	GRCh37
NC_000011.8:g.125646234G>A	NCBI36
NG_028029.1:g.7090G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-308G>A
ENST00000532101.6:n.46-91G>A
ENST00000532125.2:c.86-308G>A	ENSP00000434178.2:n.86-308G>A
ENST00000533839.6:c.85+1838G>A	ENSP00000509952.1:n.85+1838G>A
ENST00000534011.6:n.145-91G>A
ENST00000685484.1:c.86-308G>A	ENSP00000510622.1:n.86-308G>A
ENST00000685601.1:c.86-308G>A	ENSP00000510603.1:n.86-308G>A
ENST00000685765.1:c.86-308G>A	ENSP00000509991.1:n.86-308G>A
ENST00000685844.1:c.85+1838G>A	ENSP00000509820.1:n.85+1838G>A
ENST00000685857.1:n.264-308G>A
ENST00000686242.1:c.85+1838G>A	ENSP00000508950.1:n.85+1838G>A
ENST00000686888.1:c.86-308G>A	ENSP00000509619.1:n.86-308G>A
ENST00000687699.1:c.210-308G>A	ENSP00000508878.1:n.210-308G>A
ENST00000687786.1:n.1111G>A
ENST00000688588.1:c.86-308G>A	ENSP00000510802.1:n.86-308G>A
ENST00000688927.1:n.264-308G>A
ENST00000689283.1:c.209+1714G>A	ENSP00000509050.1:n.209+1714G>A
ENST00000689477.1:c.86-91G>A	ENSP00000508945.1:n.86-91G>A
ENST00000689765.1:c.85+1838G>A	ENSP00000509625.1:n.85+1838G>A
ENST00000690512.1:c.86-1349G>A	ENSP00000509793.1:n.86-1349G>A
ENST00000692039.1:c.86-222G>A	ENSP00000508821.1:n.86-222G>A
ENST00000692336.1:c.86-308G>A	ENSP00000508540.1:n.86-308G>A
ENST00000693133.1:n.225+1714G>A
ENST00000263578.10:c.86-308G>A MANE Select	ENSP00000263578.5:n.86-308G>A
ENST00000263578.9:c.86-308G>A	ENSP00000263578.5:n.86-308G>A
ENST00000524751.5:n.222+1714G>A
ENST00000525083.5:n.121+1838G>A
ENST00000525770.5:c.85+1838G>A	ENSP00000434739.1:n.85+1838G>A
ENST00000526366.5:n.101-590G>A
ENST00000526525.1:n.245+1714G>A
ENST00000527004.5:c.86-308G>A	ENSP00000436374.1:n.86-308G>A
ENST00000529802.1:n.136-308G>A
ENST00000532101.5:n.92-91G>A
ENST00000532125.1:c.44-308G>A	ENSP00000434178.1:n.44-308G>A
ENST00000533839.5:n.237+1838G>A
ENST00000534011.5:n.158-1349G>A
ENST00000534315.5:n.185G>A
NM_017547.3:c.86-308G>A	NP_060017.1:n.86-308G>A
NR_037647.1:n.252+1838G>A
NR_037648.1:n.272-308G>A
XM_006718880.2:c.-761G>A	XP_006718943.1:n.-761G>A
XM_006718881.2:c.-233+1838G>A	XP_006718944.1:n.-233+1838G>A
XM_011542895.1:c.-642-91G>A	XP_011541197.1:n.-642-91G>A
XM_011542896.1:c.-445-308G>A	XP_011541198.1:n.-445-308G>A
XM_006718881.3:c.-233+1838G>A	XP_006718944.1:n.-233+1838G>A
XM_011542895.2:c.-642-91G>A	XP_011541197.1:n.-642-91G>A
XM_011542896.2:c.-445-308G>A	XP_011541198.1:n.-445-308G>A
XM_017018000.2:c.86-308G>A	XP_016873489.1:n.86-308G>A
XM_017018001.1:c.-445-308G>A	XP_016873490.1:n.-445-308G>A
XM_017018002.1:c.-225+1838G>A	XP_016873491.1:n.-225+1838G>A
XM_017018003.2:c.-453-308G>A	XP_016873492.1:n.-453-308G>A
XM_017018004.1:c.-670-91G>A	XP_016873493.1:n.-670-91G>A
XM_017018005.1:c.-959G>A	XP_016873494.1:n.-959G>A
XM_017018006.2:c.-453-308G>A	XP_016873495.1:n.-453-308G>A
NM_017547.4:c.86-308G>A MANE Select	NP_060017.1:n.86-308G>A
NR_037647.2:n.138+1838G>A
NR_037648.2:n.263-308G>A