Canonical Allele Identifier: CA477515916
Gene: FOXRED1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.126145223G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.126275328G>A , CM000673.2:g.126275328G>A GRCh38
NC_000011.9:g.126145223G>A , CM000673.1:g.126145223G>A GRCh37
NC_000011.8:g.125650433G>A NCBI36
NG_028029.1:g.11289G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000525083.6:n.1116G>A
ENST00000532101.6:n.735G>A
ENST00000532125.2:c.630G>A ENSP00000434178.2:p.Gly210=
ENST00000533839.6:c.86-466G>A ENSP00000509952.1:n.86-466G>A
ENST00000534011.6:n.925G>A
ENST00000685484.1:c.633G>A ENSP00000510622.1:p.Gly211=
ENST00000685601.1:c.633G>A ENSP00000510603.1:p.Gly211=
ENST00000685765.1:c.633G>A ENSP00000509991.1:p.Gly211=
ENST00000685844.1:c.*170G>A ENSP00000509820.1:n.*170G>A
ENST00000685857.1:n.1372G>A
ENST00000686242.1:c.432G>A ENSP00000508950.1:n.432G>A
ENST00000686888.1:c.*200G>A ENSP00000509619.1:n.*200G>A
ENST00000687699.1:c.757G>A ENSP00000508878.1:n.757G>A
ENST00000687786.1:n.2069G>A
ENST00000688100.1:n.1554G>A
ENST00000688588.1:c.633G>A ENSP00000510802.1:p.Gly211=
ENST00000688927.1:n.2844G>A
ENST00000689283.1:c.*296G>A ENSP00000509050.1:n.*296G>A
ENST00000689477.1:c.*526G>A ENSP00000508945.1:n.*526G>A
ENST00000689765.1:c.*169-43G>A ENSP00000509625.1:n.*169-43G>A
ENST00000690512.1:c.*484G>A ENSP00000509793.1:n.*484G>A
ENST00000692039.1:c.*431G>A ENSP00000508821.1:n.*431G>A
ENST00000692336.1:c.657G>A ENSP00000508540.1:p.Gly219=
ENST00000693133.1:n.1113G>A
ENST00000263578.10:c.633G>A MANE Select ENSP00000263578.5:p.Gly211=
ENST00000263578.9:c.633G>A ENSP00000263578.5:p.Gly211=
ENST00000524751.5:n.874G>A
ENST00000525083.5:n.353G>A
ENST00000525770.5:c.*265G>A ENSP00000434739.1:n.*265G>A
ENST00000527004.5:c.535G>A ENSP00000436374.1:p.Asp179Asn
ENST00000530642.1:n.1415G>A
ENST00000532101.5:n.856G>A
ENST00000532125.1:c.591G>A ENSP00000434178.1:p.Gly197=
ENST00000533395.5:n.366G>A
ENST00000533839.5:n.238-466G>A
ENST00000534011.5:n.685G>A
ENST00000534315.5:n.945G>A
NM_017547.3:c.633G>A NP_060017.1:p.Gly211=
NR_037647.1:n.579G>A
NR_037648.1:n.819G>A
XM_006718879.2:c.123G>A XP_006718942.1:p.Gly41=
XM_006718880.2:c.-1G>A XP_006718943.1:n.-1G>A
XM_006718881.2:c.-1G>A XP_006718944.1:n.-1G>A
XM_011542895.1:c.123G>A XP_011541197.1:p.Gly41=
XM_011542896.1:c.123G>A XP_011541198.1:p.Gly41=
XM_006718879.3:c.123G>A XP_006718942.1:p.Gly41=
XM_006718881.3:c.-1G>A XP_006718944.1:n.-1G>A
XM_011542895.2:c.123G>A XP_011541197.1:p.Gly41=
XM_011542896.2:c.123G>A XP_011541198.1:p.Gly41=
XM_017018000.2:c.633G>A XP_016873489.1:p.Gly211=
XM_017018001.1:c.123G>A XP_016873490.1:p.Gly41=
XM_017018002.1:c.123G>A XP_016873491.1:p.Gly41=
XM_017018003.2:c.-1G>A XP_016873492.1:n.-1G>A
XM_017018004.1:c.-1G>A XP_016873493.1:n.-1G>A
XM_017018005.1:c.-1G>A XP_016873494.1:n.-1G>A
XM_017018006.2:c.-1G>A XP_016873495.1:n.-1G>A
NM_017547.4:c.633G>A MANE Select NP_060017.1:p.Gly211=
NR_037647.2:n.465G>A
NR_037648.2:n.810G>A