Canonical Allele Identifier: CA6354122

Gene: FOXRED1

Linked Data

• dbSNP Id: rs748079802
• ExAC: 11:126144801 C / T
• gnomAD v2: 11-126144801-C-T
• gnomAD v4: 11-126274906-C-T
• MyVariant Identifiers: chr11:g.126144801C>T (hg19) ; chr11:g.126274906C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274906C>T , CM000673.2:g.126274906C>T	GRCh38
NC_000011.9:g.126144801C>T , CM000673.1:g.126144801C>T	GRCh37
NC_000011.8:g.125650011C>T	NCBI36
NG_028029.1:g.10867C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.715-21C>T
ENST00000532101.6:n.734-421C>T
ENST00000532125.2:c.534-21C>T	ENSP00000434178.2:n.534-21C>T
ENST00000533839.6:c.86-888C>T	ENSP00000509952.1:n.86-888C>T
ENST00000534011.6:n.833-25C>T
ENST00000685484.1:c.537-21C>T	ENSP00000510622.1:n.537-21C>T
ENST00000685601.1:c.537-21C>T	ENSP00000510603.1:n.537-21C>T
ENST00000685765.1:c.537-21C>T	ENSP00000509991.1:n.537-21C>T
ENST00000685844.1:c.*169-421C>T	ENSP00000509820.1:n.*169-421C>T
ENST00000685857.1:n.971-21C>T
ENST00000686242.1:c.336-21C>T	ENSP00000508950.1:n.336-21C>T
ENST00000686888.1:c.*104-21C>T	ENSP00000509619.1:n.*104-21C>T
ENST00000687699.1:c.661-21C>T	ENSP00000508878.1:n.661-21C>T
ENST00000687786.1:n.2068-421C>T
ENST00000688100.1:n.1458-21C>T
ENST00000688588.1:c.537-21C>T	ENSP00000510802.1:n.537-21C>T
ENST00000688927.1:n.2422C>T
ENST00000689283.1:c.*200-21C>T	ENSP00000509050.1:n.*200-21C>T
ENST00000689477.1:c.*430-21C>T	ENSP00000508945.1:n.*430-21C>T
ENST00000689765.1:c.*169-465C>T	ENSP00000509625.1:n.*169-465C>T
ENST00000690512.1:c.*392-25C>T	ENSP00000509793.1:n.*392-25C>T
ENST00000692039.1:c.*335-21C>T	ENSP00000508821.1:n.*335-21C>T
ENST00000692336.1:c.561-21C>T	ENSP00000508540.1:n.561-21C>T
ENST00000693133.1:n.712-21C>T
ENST00000263578.10:c.537-21C>T MANE Select	ENSP00000263578.5:n.537-21C>T
ENST00000263578.9:c.537-21C>T	ENSP00000263578.5:n.537-21C>T
ENST00000524751.5:n.473-21C>T
ENST00000525083.5:n.352-421C>T
ENST00000525770.5:c.*169-21C>T	ENSP00000434739.1:n.*169-21C>T
ENST00000526366.5:n.468-21C>T
ENST00000527004.5:c.534-421C>T	ENSP00000436374.1:n.534-421C>T
ENST00000527875.1:n.367-21C>T
ENST00000530642.1:n.993C>T
ENST00000532101.5:n.760-21C>T
ENST00000532125.1:c.495-21C>T	ENSP00000434178.1:n.495-21C>T
ENST00000533395.5:n.365-421C>T
ENST00000533839.5:n.238-888C>T
ENST00000534011.5:n.593-25C>T
ENST00000534315.5:n.944-421C>T
NM_017547.3:c.537-21C>T	NP_060017.1:n.537-21C>T
NR_037647.1:n.483-21C>T
NR_037648.1:n.723-21C>T
XM_006718879.2:c.27-21C>T	XP_006718942.1:n.27-21C>T
XM_006718880.2:c.-2-421C>T	XP_006718943.1:n.-2-421C>T
XM_006718881.2:c.-2-421C>T	XP_006718944.1:n.-2-421C>T
XM_011542895.1:c.27-21C>T	XP_011541197.1:n.27-21C>T
XM_011542896.1:c.27-21C>T	XP_011541198.1:n.27-21C>T
XM_006718879.3:c.27-21C>T	XP_006718942.1:n.27-21C>T
XM_006718881.3:c.-2-421C>T	XP_006718944.1:n.-2-421C>T
XM_011542895.2:c.27-21C>T	XP_011541197.1:n.27-21C>T
XM_011542896.2:c.27-21C>T	XP_011541198.1:n.27-21C>T
XM_017018000.2:c.537-21C>T	XP_016873489.1:n.537-21C>T
XM_017018001.1:c.27-21C>T	XP_016873490.1:n.27-21C>T
XM_017018002.1:c.27-21C>T	XP_016873491.1:n.27-21C>T
XM_017018003.2:c.-2-421C>T	XP_016873492.1:n.-2-421C>T
XM_017018004.1:c.-2-421C>T	XP_016873493.1:n.-2-421C>T
XM_017018005.1:c.-2-421C>T	XP_016873494.1:n.-2-421C>T
XM_017018006.2:c.-2-421C>T	XP_016873495.1:n.-2-421C>T
NM_017547.4:c.537-21C>T MANE Select	NP_060017.1:n.537-21C>T
NR_037647.2:n.369-21C>T
NR_037648.2:n.714-21C>T