Canonical Allele Identifier: CA383230141

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1951100388
• gnomAD v3: 11-126275358-G-A
• gnomAD v4: 11-126275358-G-A
• MyVariant Identifiers: chr11:g.126145253G>A (hg19) ; chr11:g.126275358G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275358G>A , CM000673.2:g.126275358G>A	GRCh38
NC_000011.9:g.126145253G>A , CM000673.1:g.126145253G>A	GRCh37
NC_000011.8:g.125650463G>A	NCBI36
NG_028029.1:g.11319G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1146G>A
ENST00000532101.6:n.765G>A
ENST00000532125.2:c.660G>A	ENSP00000434178.2:p.Trp220Ter
ENST00000533839.6:c.86-436G>A	ENSP00000509952.1:n.86-436G>A
ENST00000534011.6:n.955G>A
ENST00000685484.1:c.663G>A	ENSP00000510622.1:p.Trp221Ter
ENST00000685601.1:c.663G>A	ENSP00000510603.1:p.Trp221Ter
ENST00000685765.1:c.663G>A	ENSP00000509991.1:p.Trp221Ter
ENST00000685844.1:c.*200G>A	ENSP00000509820.1:n.*200G>A
ENST00000685857.1:n.1402G>A
ENST00000686242.1:c.462G>A	ENSP00000508950.1:n.462G>A
ENST00000686888.1:c.*230G>A	ENSP00000509619.1:n.*230G>A
ENST00000687699.1:c.787G>A	ENSP00000508878.1:n.787G>A
ENST00000687786.1:n.2099G>A
ENST00000688100.1:n.1584G>A
ENST00000688588.1:c.663G>A	ENSP00000510802.1:p.Trp221Ter
ENST00000688927.1:n.2874G>A
ENST00000689283.1:c.*326G>A	ENSP00000509050.1:n.*326G>A
ENST00000689477.1:c.*556G>A	ENSP00000508945.1:n.*556G>A
ENST00000689765.1:c.*169-13G>A	ENSP00000509625.1:n.*169-13G>A
ENST00000690512.1:c.*514G>A	ENSP00000509793.1:n.*514G>A
ENST00000692039.1:c.*461G>A	ENSP00000508821.1:n.*461G>A
ENST00000692336.1:c.687G>A	ENSP00000508540.1:p.Trp229Ter
ENST00000693133.1:n.1143G>A
ENST00000263578.10:c.663G>A MANE Select	ENSP00000263578.5:p.Trp221Ter
ENST00000263578.9:c.663G>A	ENSP00000263578.5:p.Trp221Ter
ENST00000525083.5:n.383G>A
ENST00000525770.5:c.*295G>A	ENSP00000434739.1:n.*295G>A
ENST00000527004.5:c.*7G>A	ENSP00000436374.1:n.*7G>A
ENST00000530642.1:n.1445G>A
ENST00000532101.5:n.886G>A
ENST00000532125.1:c.621G>A	ENSP00000434178.1:p.Trp207Ter
ENST00000533395.5:n.396G>A
ENST00000533839.5:n.238-436G>A
ENST00000534011.5:n.715G>A
ENST00000534315.5:n.975G>A
NM_017547.3:c.663G>A	NP_060017.1:p.Trp221Ter
NR_037647.1:n.609G>A
NR_037648.1:n.849G>A
XM_006718879.2:c.153G>A	XP_006718942.1:p.Trp51Ter
XM_006718880.2:c.30G>A	XP_006718943.1:p.Trp10Ter
XM_006718881.2:c.30G>A	XP_006718944.1:p.Trp10Ter
XM_011542895.1:c.153G>A	XP_011541197.1:p.Trp51Ter
XM_011542896.1:c.153G>A	XP_011541198.1:p.Trp51Ter
XM_006718879.3:c.153G>A	XP_006718942.1:p.Trp51Ter
XM_006718881.3:c.30G>A	XP_006718944.1:p.Trp10Ter
XM_011542895.2:c.153G>A	XP_011541197.1:p.Trp51Ter
XM_011542896.2:c.153G>A	XP_011541198.1:p.Trp51Ter
XM_017018000.2:c.663G>A	XP_016873489.1:p.Trp221Ter
XM_017018001.1:c.153G>A	XP_016873490.1:p.Trp51Ter
XM_017018002.1:c.153G>A	XP_016873491.1:p.Trp51Ter
XM_017018003.2:c.30G>A	XP_016873492.1:p.Trp10Ter
XM_017018004.1:c.30G>A	XP_016873493.1:p.Trp10Ter
XM_017018005.1:c.30G>A	XP_016873494.1:p.Trp10Ter
XM_017018006.2:c.30G>A	XP_016873495.1:p.Trp10Ter
NM_017547.4:c.663G>A MANE Select	NP_060017.1:p.Trp221Ter
NR_037647.2:n.495G>A
NR_037648.2:n.840G>A