Canonical Allele Identifier: CA230563121

Gene: FOXRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126277506G>A , CM000673.2:g.126277506G>A	GRCh38
NC_000011.9:g.126147401G>A , CM000673.1:g.126147401G>A	GRCh37
NC_000011.8:g.125652611G>A	NCBI36
NG_028029.1:g.13467G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1761G>A
ENST00000532101.6:n.1407G>A
ENST00000532125.2:c.1275G>A	ENSP00000434178.2:p.Pro425=
ENST00000533839.6:c.630G>A	ENSP00000509952.1:p.Pro210=
ENST00000534011.6:n.1511G>A
ENST00000685484.1:c.*274G>A	ENSP00000510622.1:n.*274G>A
ENST00000685601.1:c.*330G>A	ENSP00000510603.1:n.*330G>A
ENST00000685765.1:c.*266G>A	ENSP00000509991.1:n.*266G>A
ENST00000685844.1:c.*888G>A	ENSP00000509820.1:n.*888G>A
ENST00000685857.1:n.2382G>A
ENST00000686242.1:c.1077G>A	ENSP00000508950.1:n.1077G>A
ENST00000686888.1:c.*845G>A	ENSP00000509619.1:n.*845G>A
ENST00000687699.1:c.1402G>A	ENSP00000508878.1:n.1402G>A
ENST00000687786.1:n.2714G>A
ENST00000688100.1:n.2171G>A
ENST00000688588.1:c.*98G>A	ENSP00000510802.1:n.*98G>A
ENST00000688927.1:n.3489G>A
ENST00000689283.1:c.*941G>A	ENSP00000509050.1:n.*941G>A
ENST00000689477.1:c.*1171G>A	ENSP00000508945.1:n.*1171G>A
ENST00000689765.1:c.*771G>A	ENSP00000509625.1:n.*771G>A
ENST00000690512.1:c.*1129G>A	ENSP00000509793.1:n.*1129G>A
ENST00000692039.1:c.*1103G>A	ENSP00000508821.1:n.*1103G>A
ENST00000692336.1:c.1302G>A	ENSP00000508540.1:p.Pro434=
ENST00000693133.1:n.2123G>A
ENST00000263578.10:c.1278G>A MANE Select	ENSP00000263578.5:p.Pro426=
ENST00000263578.9:c.1278G>A	ENSP00000263578.5:p.Pro426=
ENST00000525083.5:n.1071G>A
ENST00000525770.5:c.*910G>A	ENSP00000434739.1:n.*910G>A
ENST00000527004.5:c.*622G>A	ENSP00000436374.1:n.*622G>A
ENST00000530642.1:n.2425G>A
ENST00000532125.1:c.1236G>A	ENSP00000434178.1:p.Pro412=
ENST00000532590.1:n.336G>A
ENST00000534011.5:n.1330G>A
ENST00000534315.5:n.1590G>A
NM_017547.3:c.1278G>A	NP_060017.1:p.Pro426=
NR_037647.1:n.1224G>A
NR_037648.1:n.1464G>A
XM_006718879.2:c.768G>A	XP_006718942.1:p.Pro256=
XM_006718880.2:c.645G>A	XP_006718943.1:p.Pro215=
XM_006718881.2:c.645G>A	XP_006718944.1:p.Pro215=
XM_011542895.1:c.768G>A	XP_011541197.1:p.Pro256=
XM_011542896.1:c.768G>A	XP_011541198.1:p.Pro256=
XM_006718879.3:c.768G>A	XP_006718942.1:p.Pro256=
XM_006718881.3:c.645G>A	XP_006718944.1:p.Pro215=
XM_011542895.2:c.768G>A	XP_011541197.1:p.Pro256=
XM_011542896.2:c.768G>A	XP_011541198.1:p.Pro256=
XM_017018000.2:c.1275G>A	XP_016873489.1:p.Pro425=
XM_017018001.1:c.768G>A	XP_016873490.1:p.Pro256=
XM_017018002.1:c.768G>A	XP_016873491.1:p.Pro256=
XM_017018003.2:c.645G>A	XP_016873492.1:p.Pro215=
XM_017018004.1:c.645G>A	XP_016873493.1:p.Pro215=
XM_017018005.1:c.645G>A	XP_016873494.1:p.Pro215=
XM_017018006.2:c.642G>A	XP_016873495.1:p.Pro214=
NM_017547.4:c.1278G>A MANE Select	NP_060017.1:p.Pro426=
NR_037647.2:n.1110G>A
NR_037648.2:n.1455G>A