Canonical Allele Identifier: CA2616727169

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126271188-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126271188G>T , CM000673.2:g.126271188G>T	GRCh38
NC_000011.9:g.126141083G>T , CM000673.1:g.126141083G>T	GRCh37
NC_000011.8:g.125646293G>T	NCBI36
NG_028029.1:g.7149G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.264-249G>T
ENST00000532101.6:n.46-32G>T
ENST00000532125.2:c.86-249G>T	ENSP00000434178.2:n.86-249G>T
ENST00000533839.6:c.85+1897G>T	ENSP00000509952.1:n.85+1897G>T
ENST00000534011.6:n.145-32G>T
ENST00000685484.1:c.86-249G>T	ENSP00000510622.1:n.86-249G>T
ENST00000685601.1:c.86-249G>T	ENSP00000510603.1:n.86-249G>T
ENST00000685765.1:c.86-249G>T	ENSP00000509991.1:n.86-249G>T
ENST00000685844.1:c.86-1781G>T	ENSP00000509820.1:n.86-1781G>T
ENST00000685857.1:n.264-249G>T
ENST00000686242.1:c.86-1781G>T	ENSP00000508950.1:n.86-1781G>T
ENST00000686888.1:c.86-249G>T	ENSP00000509619.1:n.86-249G>T
ENST00000687699.1:c.210-249G>T	ENSP00000508878.1:n.210-249G>T
ENST00000687786.1:n.1170G>T
ENST00000688588.1:c.86-249G>T	ENSP00000510802.1:n.86-249G>T
ENST00000688927.1:n.264-249G>T
ENST00000689283.1:c.209+1773G>T	ENSP00000509050.1:n.209+1773G>T
ENST00000689477.1:c.86-32G>T	ENSP00000508945.1:n.86-32G>T
ENST00000689765.1:c.86-1781G>T	ENSP00000509625.1:n.86-1781G>T
ENST00000690512.1:c.86-1290G>T	ENSP00000509793.1:n.86-1290G>T
ENST00000692039.1:c.86-163G>T	ENSP00000508821.1:n.86-163G>T
ENST00000692336.1:c.86-249G>T	ENSP00000508540.1:n.86-249G>T
ENST00000693133.1:n.225+1773G>T
ENST00000263578.10:c.86-249G>T MANE Select	ENSP00000263578.5:n.86-249G>T
ENST00000263578.9:c.86-249G>T	ENSP00000263578.5:n.86-249G>T
ENST00000524751.5:n.222+1773G>T
ENST00000525083.5:n.122-1781G>T
ENST00000525770.5:c.86-1781G>T	ENSP00000434739.1:n.86-1781G>T
ENST00000526366.5:n.101-531G>T
ENST00000526525.1:n.245+1773G>T
ENST00000527004.5:c.86-249G>T	ENSP00000436374.1:n.86-249G>T
ENST00000529802.1:n.136-249G>T
ENST00000532101.5:n.92-32G>T
ENST00000532125.1:c.44-249G>T	ENSP00000434178.1:n.44-249G>T
ENST00000533839.5:n.237+1897G>T
ENST00000534011.5:n.158-1290G>T
ENST00000534315.5:n.244G>T
NM_017547.3:c.86-249G>T	NP_060017.1:n.86-249G>T
NR_037647.1:n.253-1781G>T
NR_037648.1:n.272-249G>T
XM_006718880.2:c.-702G>T	XP_006718943.1:n.-702G>T
XM_006718881.2:c.-232-1781G>T	XP_006718944.1:n.-232-1781G>T
XM_011542895.1:c.-642-32G>T	XP_011541197.1:n.-642-32G>T
XM_011542896.1:c.-445-249G>T	XP_011541198.1:n.-445-249G>T
XM_006718881.3:c.-232-1781G>T	XP_006718944.1:n.-232-1781G>T
XM_011542895.2:c.-642-32G>T	XP_011541197.1:n.-642-32G>T
XM_011542896.2:c.-445-249G>T	XP_011541198.1:n.-445-249G>T
XM_017018000.2:c.86-249G>T	XP_016873489.1:n.86-249G>T
XM_017018001.1:c.-445-249G>T	XP_016873490.1:n.-445-249G>T
XM_017018002.1:c.-224-1781G>T	XP_016873491.1:n.-224-1781G>T
XM_017018003.2:c.-453-249G>T	XP_016873492.1:n.-453-249G>T
XM_017018004.1:c.-670-32G>T	XP_016873493.1:n.-670-32G>T
XM_017018005.1:c.-900G>T	XP_016873494.1:n.-900G>T
XM_017018006.2:c.-453-249G>T	XP_016873495.1:n.-453-249G>T
NM_017547.4:c.86-249G>T MANE Select	NP_060017.1:n.86-249G>T
NR_037647.2:n.139-1781G>T
NR_037648.2:n.263-249G>T