Canonical Allele Identifier: CA6354126

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 509772
• ClinVar RCV Id: RCV000614185 ; RCV001107092 ; RCV002063291
• dbSNP Id: rs199599636
• ExAC: 11:126144811 G / A
• gnomAD v2: 11-126144811-G-A
• gnomAD v3: 11-126274916-G-A
• gnomAD v4: 11-126274916-G-A
• MyVariant Identifiers: chr11:g.126144811G>A (hg19) ; chr11:g.126274916G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274916G>A , CM000673.2:g.126274916G>A	GRCh38
NC_000011.9:g.126144811G>A , CM000673.1:g.126144811G>A	GRCh37
NC_000011.8:g.125650021G>A	NCBI36
NG_028029.1:g.10877G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.715-11G>A
ENST00000532101.6:n.734-411G>A
ENST00000532125.2:c.534-11G>A	ENSP00000434178.2:n.534-11G>A
ENST00000533839.6:c.86-878G>A	ENSP00000509952.1:n.86-878G>A
ENST00000534011.6:n.833-15G>A
ENST00000685484.1:c.537-11G>A	ENSP00000510622.1:n.537-11G>A
ENST00000685601.1:c.537-11G>A	ENSP00000510603.1:n.537-11G>A
ENST00000685765.1:c.537-11G>A	ENSP00000509991.1:n.537-11G>A
ENST00000685844.1:c.*169-411G>A	ENSP00000509820.1:n.*169-411G>A
ENST00000685857.1:n.971-11G>A
ENST00000686242.1:c.336-11G>A	ENSP00000508950.1:n.336-11G>A
ENST00000686888.1:c.*104-11G>A	ENSP00000509619.1:n.*104-11G>A
ENST00000687699.1:c.661-11G>A	ENSP00000508878.1:n.661-11G>A
ENST00000687786.1:n.2068-411G>A
ENST00000688100.1:n.1458-11G>A
ENST00000688588.1:c.537-11G>A	ENSP00000510802.1:n.537-11G>A
ENST00000688927.1:n.2432G>A
ENST00000689283.1:c.*200-11G>A	ENSP00000509050.1:n.*200-11G>A
ENST00000689477.1:c.*430-11G>A	ENSP00000508945.1:n.*430-11G>A
ENST00000689765.1:c.*169-455G>A	ENSP00000509625.1:n.*169-455G>A
ENST00000690512.1:c.*392-15G>A	ENSP00000509793.1:n.*392-15G>A
ENST00000692039.1:c.*335-11G>A	ENSP00000508821.1:n.*335-11G>A
ENST00000692336.1:c.561-11G>A	ENSP00000508540.1:n.561-11G>A
ENST00000693133.1:n.712-11G>A
ENST00000263578.10:c.537-11G>A MANE Select	ENSP00000263578.5:n.537-11G>A
ENST00000263578.9:c.537-11G>A	ENSP00000263578.5:n.537-11G>A
ENST00000524751.5:n.473-11G>A
ENST00000525083.5:n.352-411G>A
ENST00000525770.5:c.*169-11G>A	ENSP00000434739.1:n.*169-11G>A
ENST00000526366.5:n.468-11G>A
ENST00000527004.5:c.534-411G>A	ENSP00000436374.1:n.534-411G>A
ENST00000527875.1:n.367-11G>A
ENST00000530642.1:n.1003G>A
ENST00000532101.5:n.760-11G>A
ENST00000532125.1:c.495-11G>A	ENSP00000434178.1:n.495-11G>A
ENST00000533395.5:n.365-411G>A
ENST00000533839.5:n.238-878G>A
ENST00000534011.5:n.593-15G>A
ENST00000534315.5:n.944-411G>A
NM_017547.3:c.537-11G>A	NP_060017.1:n.537-11G>A
NR_037647.1:n.483-11G>A
NR_037648.1:n.723-11G>A
XM_006718879.2:c.27-11G>A	XP_006718942.1:n.27-11G>A
XM_006718880.2:c.-2-411G>A	XP_006718943.1:n.-2-411G>A
XM_006718881.2:c.-2-411G>A	XP_006718944.1:n.-2-411G>A
XM_011542895.1:c.27-11G>A	XP_011541197.1:n.27-11G>A
XM_011542896.1:c.27-11G>A	XP_011541198.1:n.27-11G>A
XM_006718879.3:c.27-11G>A	XP_006718942.1:n.27-11G>A
XM_006718881.3:c.-2-411G>A	XP_006718944.1:n.-2-411G>A
XM_011542895.2:c.27-11G>A	XP_011541197.1:n.27-11G>A
XM_011542896.2:c.27-11G>A	XP_011541198.1:n.27-11G>A
XM_017018000.2:c.537-11G>A	XP_016873489.1:n.537-11G>A
XM_017018001.1:c.27-11G>A	XP_016873490.1:n.27-11G>A
XM_017018002.1:c.27-11G>A	XP_016873491.1:n.27-11G>A
XM_017018003.2:c.-2-411G>A	XP_016873492.1:n.-2-411G>A
XM_017018004.1:c.-2-411G>A	XP_016873493.1:n.-2-411G>A
XM_017018005.1:c.-2-411G>A	XP_016873494.1:n.-2-411G>A
XM_017018006.2:c.-2-411G>A	XP_016873495.1:n.-2-411G>A
NM_017547.4:c.537-11G>A MANE Select	NP_060017.1:n.537-11G>A
NR_037647.2:n.369-11G>A
NR_037648.2:n.714-11G>A