Canonical Allele Identifier: CA383230105

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275341-G-T
• MyVariant Identifiers: chr11:g.126145236G>T (hg19) ; chr11:g.126275341G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275341G>T , CM000673.2:g.126275341G>T	GRCh38
NC_000011.9:g.126145236G>T , CM000673.1:g.126145236G>T	GRCh37
NC_000011.8:g.125650446G>T	NCBI36
NG_028029.1:g.11302G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1129G>T
ENST00000532101.6:n.748G>T
ENST00000532125.2:c.643G>T	ENSP00000434178.2:p.Gly215Cys
ENST00000533839.6:c.86-453G>T	ENSP00000509952.1:n.86-453G>T
ENST00000534011.6:n.938G>T
ENST00000685484.1:c.646G>T	ENSP00000510622.1:p.Gly216Cys
ENST00000685601.1:c.646G>T	ENSP00000510603.1:p.Gly216Cys
ENST00000685765.1:c.646G>T	ENSP00000509991.1:p.Gly216Cys
ENST00000685844.1:c.*183G>T	ENSP00000509820.1:n.*183G>T
ENST00000685857.1:n.1385G>T
ENST00000686242.1:c.445G>T	ENSP00000508950.1:n.445G>T
ENST00000686888.1:c.*213G>T	ENSP00000509619.1:n.*213G>T
ENST00000687699.1:c.770G>T	ENSP00000508878.1:n.770G>T
ENST00000687786.1:n.2082G>T
ENST00000688100.1:n.1567G>T
ENST00000688588.1:c.646G>T	ENSP00000510802.1:p.Gly216Cys
ENST00000688927.1:n.2857G>T
ENST00000689283.1:c.*309G>T	ENSP00000509050.1:n.*309G>T
ENST00000689477.1:c.*539G>T	ENSP00000508945.1:n.*539G>T
ENST00000689765.1:c.*169-30G>T	ENSP00000509625.1:n.*169-30G>T
ENST00000690512.1:c.*497G>T	ENSP00000509793.1:n.*497G>T
ENST00000692039.1:c.*444G>T	ENSP00000508821.1:n.*444G>T
ENST00000692336.1:c.670G>T	ENSP00000508540.1:p.Gly224Cys
ENST00000693133.1:n.1126G>T
ENST00000263578.10:c.646G>T MANE Select	ENSP00000263578.5:p.Gly216Cys
ENST00000263578.9:c.646G>T	ENSP00000263578.5:p.Gly216Cys
ENST00000524751.5:n.887G>T
ENST00000525083.5:n.366G>T
ENST00000525770.5:c.*278G>T	ENSP00000434739.1:n.*278G>T
ENST00000527004.5:c.548G>T	ENSP00000436374.1:p.Arg183Met
ENST00000530642.1:n.1428G>T
ENST00000532101.5:n.869G>T
ENST00000532125.1:c.604G>T	ENSP00000434178.1:p.Gly202Cys
ENST00000533395.5:n.379G>T
ENST00000533839.5:n.238-453G>T
ENST00000534011.5:n.698G>T
ENST00000534315.5:n.958G>T
NM_017547.3:c.646G>T	NP_060017.1:p.Gly216Cys
NR_037647.1:n.592G>T
NR_037648.1:n.832G>T
XM_006718879.2:c.136G>T	XP_006718942.1:p.Gly46Cys
XM_006718880.2:c.13G>T	XP_006718943.1:p.Gly5Cys
XM_006718881.2:c.13G>T	XP_006718944.1:p.Gly5Cys
XM_011542895.1:c.136G>T	XP_011541197.1:p.Gly46Cys
XM_011542896.1:c.136G>T	XP_011541198.1:p.Gly46Cys
XM_006718879.3:c.136G>T	XP_006718942.1:p.Gly46Cys
XM_006718881.3:c.13G>T	XP_006718944.1:p.Gly5Cys
XM_011542895.2:c.136G>T	XP_011541197.1:p.Gly46Cys
XM_011542896.2:c.136G>T	XP_011541198.1:p.Gly46Cys
XM_017018000.2:c.646G>T	XP_016873489.1:p.Gly216Cys
XM_017018001.1:c.136G>T	XP_016873490.1:p.Gly46Cys
XM_017018002.1:c.136G>T	XP_016873491.1:p.Gly46Cys
XM_017018003.2:c.13G>T	XP_016873492.1:p.Gly5Cys
XM_017018004.1:c.13G>T	XP_016873493.1:p.Gly5Cys
XM_017018005.1:c.13G>T	XP_016873494.1:p.Gly5Cys
XM_017018006.2:c.13G>T	XP_016873495.1:p.Gly5Cys
NM_017547.4:c.646G>T MANE Select	NP_060017.1:p.Gly216Cys
NR_037647.2:n.478G>T
NR_037648.2:n.823G>T