Canonical Allele Identifier: CA2616722193

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126274921-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274921T>C , CM000673.2:g.126274921T>C	GRCh38
NC_000011.9:g.126144816T>C , CM000673.1:g.126144816T>C	GRCh37
NC_000011.8:g.125650026T>C	NCBI36
NG_028029.1:g.10882T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.715-6T>C
ENST00000532101.6:n.734-406T>C
ENST00000532125.2:c.534-6T>C	ENSP00000434178.2:n.534-6T>C
ENST00000533839.6:c.86-873T>C	ENSP00000509952.1:n.86-873T>C
ENST00000534011.6:n.833-10T>C
ENST00000685484.1:c.537-6T>C	ENSP00000510622.1:n.537-6T>C
ENST00000685601.1:c.537-6T>C	ENSP00000510603.1:n.537-6T>C
ENST00000685765.1:c.537-6T>C	ENSP00000509991.1:n.537-6T>C
ENST00000685844.1:c.*169-406T>C	ENSP00000509820.1:n.*169-406T>C
ENST00000685857.1:n.971-6T>C
ENST00000686242.1:c.336-6T>C	ENSP00000508950.1:n.336-6T>C
ENST00000686888.1:c.*104-6T>C	ENSP00000509619.1:n.*104-6T>C
ENST00000687699.1:c.661-6T>C	ENSP00000508878.1:n.661-6T>C
ENST00000687786.1:n.2068-406T>C
ENST00000688100.1:n.1458-6T>C
ENST00000688588.1:c.537-6T>C	ENSP00000510802.1:n.537-6T>C
ENST00000688927.1:n.2437T>C
ENST00000689283.1:c.*200-6T>C	ENSP00000509050.1:n.*200-6T>C
ENST00000689477.1:c.*430-6T>C	ENSP00000508945.1:n.*430-6T>C
ENST00000689765.1:c.*169-450T>C	ENSP00000509625.1:n.*169-450T>C
ENST00000690512.1:c.*392-10T>C	ENSP00000509793.1:n.*392-10T>C
ENST00000692039.1:c.*335-6T>C	ENSP00000508821.1:n.*335-6T>C
ENST00000692336.1:c.561-6T>C	ENSP00000508540.1:n.561-6T>C
ENST00000693133.1:n.712-6T>C
ENST00000263578.10:c.537-6T>C MANE Select	ENSP00000263578.5:n.537-6T>C
ENST00000263578.9:c.537-6T>C	ENSP00000263578.5:n.537-6T>C
ENST00000524751.5:n.473-6T>C
ENST00000525083.5:n.352-406T>C
ENST00000525770.5:c.*169-6T>C	ENSP00000434739.1:n.*169-6T>C
ENST00000526366.5:n.468-6T>C
ENST00000527004.5:c.534-406T>C	ENSP00000436374.1:n.534-406T>C
ENST00000527875.1:n.367-6T>C
ENST00000530642.1:n.1008T>C
ENST00000532101.5:n.760-6T>C
ENST00000532125.1:c.495-6T>C	ENSP00000434178.1:n.495-6T>C
ENST00000533395.5:n.365-406T>C
ENST00000533839.5:n.238-873T>C
ENST00000534011.5:n.593-10T>C
ENST00000534315.5:n.944-406T>C
NM_017547.3:c.537-6T>C	NP_060017.1:n.537-6T>C
NR_037647.1:n.483-6T>C
NR_037648.1:n.723-6T>C
XM_006718879.2:c.27-6T>C	XP_006718942.1:n.27-6T>C
XM_006718880.2:c.-2-406T>C	XP_006718943.1:n.-2-406T>C
XM_006718881.2:c.-2-406T>C	XP_006718944.1:n.-2-406T>C
XM_011542895.1:c.27-6T>C	XP_011541197.1:n.27-6T>C
XM_011542896.1:c.27-6T>C	XP_011541198.1:n.27-6T>C
XM_006718879.3:c.27-6T>C	XP_006718942.1:n.27-6T>C
XM_006718881.3:c.-2-406T>C	XP_006718944.1:n.-2-406T>C
XM_011542895.2:c.27-6T>C	XP_011541197.1:n.27-6T>C
XM_011542896.2:c.27-6T>C	XP_011541198.1:n.27-6T>C
XM_017018000.2:c.537-6T>C	XP_016873489.1:n.537-6T>C
XM_017018001.1:c.27-6T>C	XP_016873490.1:n.27-6T>C
XM_017018002.1:c.27-6T>C	XP_016873491.1:n.27-6T>C
XM_017018003.2:c.-2-406T>C	XP_016873492.1:n.-2-406T>C
XM_017018004.1:c.-2-406T>C	XP_016873493.1:n.-2-406T>C
XM_017018005.1:c.-2-406T>C	XP_016873494.1:n.-2-406T>C
XM_017018006.2:c.-2-406T>C	XP_016873495.1:n.-2-406T>C
NM_017547.4:c.537-6T>C MANE Select	NP_060017.1:n.537-6T>C
NR_037647.2:n.369-6T>C
NR_037648.2:n.714-6T>C