Canonical Allele Identifier: CA2616722446

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275313-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275313T>G , CM000673.2:g.126275313T>G	GRCh38
NC_000011.9:g.126145208T>G , CM000673.1:g.126145208T>G	GRCh37
NC_000011.8:g.125650418T>G	NCBI36
NG_028029.1:g.11274T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000525083.6:n.1101T>G
ENST00000532101.6:n.734-14T>G
ENST00000532125.2:c.629-14T>G	ENSP00000434178.2:n.629-14T>G
ENST00000533839.6:c.86-481T>G	ENSP00000509952.1:n.86-481T>G
ENST00000534011.6:n.924-14T>G
ENST00000685484.1:c.632-14T>G	ENSP00000510622.1:n.632-14T>G
ENST00000685601.1:c.632-14T>G	ENSP00000510603.1:n.632-14T>G
ENST00000685765.1:c.632-14T>G	ENSP00000509991.1:n.632-14T>G
ENST00000685844.1:c.*169-14T>G	ENSP00000509820.1:n.*169-14T>G
ENST00000685857.1:n.1357T>G
ENST00000686242.1:c.431-14T>G	ENSP00000508950.1:n.431-14T>G
ENST00000686888.1:c.*199-14T>G	ENSP00000509619.1:n.*199-14T>G
ENST00000687699.1:c.756-14T>G	ENSP00000508878.1:n.756-14T>G
ENST00000687786.1:n.2068-14T>G
ENST00000688100.1:n.1553-14T>G
ENST00000688588.1:c.632-14T>G	ENSP00000510802.1:n.632-14T>G
ENST00000688927.1:n.2829T>G
ENST00000689283.1:c.*295-14T>G	ENSP00000509050.1:n.*295-14T>G
ENST00000689477.1:c.*525-14T>G	ENSP00000508945.1:n.*525-14T>G
ENST00000689765.1:c.*169-58T>G	ENSP00000509625.1:n.*169-58T>G
ENST00000690512.1:c.*483-14T>G	ENSP00000509793.1:n.*483-14T>G
ENST00000692039.1:c.*430-14T>G	ENSP00000508821.1:n.*430-14T>G
ENST00000692336.1:c.656-14T>G	ENSP00000508540.1:n.656-14T>G
ENST00000693133.1:n.1098T>G
ENST00000263578.10:c.632-14T>G MANE Select	ENSP00000263578.5:n.632-14T>G
ENST00000263578.9:c.632-14T>G	ENSP00000263578.5:n.632-14T>G
ENST00000524751.5:n.859T>G
ENST00000525083.5:n.352-14T>G
ENST00000525770.5:c.*264-14T>G	ENSP00000434739.1:n.*264-14T>G
ENST00000527004.5:c.534-14T>G	ENSP00000436374.1:n.534-14T>G
ENST00000530642.1:n.1400T>G
ENST00000532101.5:n.855-14T>G
ENST00000532125.1:c.590-14T>G	ENSP00000434178.1:n.590-14T>G
ENST00000533395.5:n.365-14T>G
ENST00000533839.5:n.238-481T>G
ENST00000534011.5:n.684-14T>G
ENST00000534315.5:n.944-14T>G
NM_017547.3:c.632-14T>G	NP_060017.1:n.632-14T>G
NR_037647.1:n.578-14T>G
NR_037648.1:n.818-14T>G
XM_006718879.2:c.122-14T>G	XP_006718942.1:n.122-14T>G
XM_006718880.2:c.-2-14T>G	XP_006718943.1:n.-2-14T>G
XM_006718881.2:c.-2-14T>G	XP_006718944.1:n.-2-14T>G
XM_011542895.1:c.122-14T>G	XP_011541197.1:n.122-14T>G
XM_011542896.1:c.122-14T>G	XP_011541198.1:n.122-14T>G
XM_006718879.3:c.122-14T>G	XP_006718942.1:n.122-14T>G
XM_006718881.3:c.-2-14T>G	XP_006718944.1:n.-2-14T>G
XM_011542895.2:c.122-14T>G	XP_011541197.1:n.122-14T>G
XM_011542896.2:c.122-14T>G	XP_011541198.1:n.122-14T>G
XM_017018000.2:c.632-14T>G	XP_016873489.1:n.632-14T>G
XM_017018001.1:c.122-14T>G	XP_016873490.1:n.122-14T>G
XM_017018002.1:c.122-14T>G	XP_016873491.1:n.122-14T>G
XM_017018003.2:c.-2-14T>G	XP_016873492.1:n.-2-14T>G
XM_017018004.1:c.-2-14T>G	XP_016873493.1:n.-2-14T>G
XM_017018005.1:c.-2-14T>G	XP_016873494.1:n.-2-14T>G
XM_017018006.2:c.-2-14T>G	XP_016873495.1:n.-2-14T>G
NM_017547.4:c.632-14T>G MANE Select	NP_060017.1:n.632-14T>G
NR_037647.2:n.464-14T>G
NR_037648.2:n.809-14T>G