Canonical Allele Identifier: CA383230167

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126275369-A-T
• MyVariant Identifiers: chr11:g.126145264A>T (hg19) ; chr11:g.126275369A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275369A>T , CM000673.2:g.126275369A>T	GRCh38
NC_000011.9:g.126145264A>T , CM000673.1:g.126145264A>T	GRCh37
NC_000011.8:g.125650474A>T	NCBI36
NG_028029.1:g.11330A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1157A>T
ENST00000532101.6:n.776A>T
ENST00000532125.2:c.671A>T	ENSP00000434178.2:p.Gln224Leu
ENST00000533839.6:c.86-425A>T	ENSP00000509952.1:n.86-425A>T
ENST00000534011.6:n.966A>T
ENST00000685484.1:c.674A>T	ENSP00000510622.1:p.Gln225Leu
ENST00000685601.1:c.674A>T	ENSP00000510603.1:p.Gln225Leu
ENST00000685765.1:c.674A>T	ENSP00000509991.1:p.Gln225Leu
ENST00000685844.1:c.*211A>T	ENSP00000509820.1:n.*211A>T
ENST00000685857.1:n.1413A>T
ENST00000686242.1:c.473A>T	ENSP00000508950.1:n.473A>T
ENST00000686888.1:c.*241A>T	ENSP00000509619.1:n.*241A>T
ENST00000687699.1:c.798A>T	ENSP00000508878.1:n.798A>T
ENST00000687786.1:n.2110A>T
ENST00000688100.1:n.1595A>T
ENST00000688588.1:c.674A>T	ENSP00000510802.1:p.Gln225Leu
ENST00000688927.1:n.2885A>T
ENST00000689283.1:c.*337A>T	ENSP00000509050.1:n.*337A>T
ENST00000689477.1:c.*567A>T	ENSP00000508945.1:n.*567A>T
ENST00000689765.1:c.*169-2A>T	ENSP00000509625.1:n.*169-2A>T
ENST00000690512.1:c.*525A>T	ENSP00000509793.1:n.*525A>T
ENST00000692039.1:c.*472A>T	ENSP00000508821.1:n.*472A>T
ENST00000692336.1:c.698A>T	ENSP00000508540.1:p.Gln233Leu
ENST00000693133.1:n.1154A>T
ENST00000263578.10:c.674A>T MANE Select	ENSP00000263578.5:p.Gln225Leu
ENST00000263578.9:c.674A>T	ENSP00000263578.5:p.Gln225Leu
ENST00000525083.5:n.394A>T
ENST00000525770.5:c.*306A>T	ENSP00000434739.1:n.*306A>T
ENST00000527004.5:c.*18A>T	ENSP00000436374.1:n.*18A>T
ENST00000530642.1:n.1456A>T
ENST00000532101.5:n.897A>T
ENST00000532125.1:c.632A>T	ENSP00000434178.1:p.Gln211Leu
ENST00000533395.5:n.407A>T
ENST00000533839.5:n.238-425A>T
ENST00000534011.5:n.726A>T
ENST00000534315.5:n.986A>T
NM_017547.3:c.674A>T	NP_060017.1:p.Gln225Leu
NR_037647.1:n.620A>T
NR_037648.1:n.860A>T
XM_006718879.2:c.164A>T	XP_006718942.1:p.Gln55Leu
XM_006718880.2:c.41A>T	XP_006718943.1:p.Gln14Leu
XM_006718881.2:c.41A>T	XP_006718944.1:p.Gln14Leu
XM_011542895.1:c.164A>T	XP_011541197.1:p.Gln55Leu
XM_011542896.1:c.164A>T	XP_011541198.1:p.Gln55Leu
XM_006718879.3:c.164A>T	XP_006718942.1:p.Gln55Leu
XM_006718881.3:c.41A>T	XP_006718944.1:p.Gln14Leu
XM_011542895.2:c.164A>T	XP_011541197.1:p.Gln55Leu
XM_011542896.2:c.164A>T	XP_011541198.1:p.Gln55Leu
XM_017018000.2:c.674A>T	XP_016873489.1:p.Gln225Leu
XM_017018001.1:c.164A>T	XP_016873490.1:p.Gln55Leu
XM_017018002.1:c.164A>T	XP_016873491.1:p.Gln55Leu
XM_017018003.2:c.41A>T	XP_016873492.1:p.Gln14Leu
XM_017018004.1:c.41A>T	XP_016873493.1:p.Gln14Leu
XM_017018005.1:c.41A>T	XP_016873494.1:p.Gln14Leu
XM_017018006.2:c.41A>T	XP_016873495.1:p.Gln14Leu
NM_017547.4:c.674A>T MANE Select	NP_060017.1:p.Gln225Leu
NR_037647.2:n.506A>T
NR_037648.2:n.851A>T