Canonical Allele Identifier: CA2007079513

Gene: FOXRED1

Linked Data

• ClinVar Variation Id: 2763096
• ClinVar RCV Id: RCV003564961
• dbSNP Id: rs1951088118

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274915_126274929del , CM000673.2:g.126274915_126274929del	GRCh38
NC_000011.9:g.126144810_126144824del , CM000673.1:g.126144810_126144824del	GRCh37
NC_000011.8:g.125650020_125650034del	NCBI36
NG_028029.1:g.10876_10890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.715-12_717del
ENST00000532101.6:n.734-412_734-398del
ENST00000532125.2:c.534-12_536del
ENST00000533839.6:c.86-879_86-865del	ENSP00000509952.1:n.86-879_86-865del
ENST00000534011.6:n.833-16_833-2del
ENST00000685484.1:c.537-12_539del
ENST00000685601.1:c.537-12_539del
ENST00000685765.1:c.537-12_539del
ENST00000685844.1:c.*169-412_*169-398del	ENSP00000509820.1:n.*169-412_*169-398del
ENST00000685857.1:n.971-12_973del
ENST00000686242.1:c.336-12_338del
ENST00000686888.1:c.*104-12_*106del
ENST00000687699.1:c.661-12_663del
ENST00000687786.1:n.2068-412_2068-398del
ENST00000688100.1:n.1458-12_1460del
ENST00000688588.1:c.537-12_539del
ENST00000688927.1:n.2431_2445del
ENST00000689283.1:c.*200-12_*202del
ENST00000689477.1:c.*430-12_*432del
ENST00000689765.1:c.*169-456_*169-442del	ENSP00000509625.1:n.*169-456_*169-442del
ENST00000690512.1:c.*392-16_*392-2del	ENSP00000509793.1:n.*392-16_*392-2del
ENST00000692039.1:c.*335-12_*337del
ENST00000692336.1:c.561-12_563del
ENST00000693133.1:n.712-12_714del
ENST00000263578.10:c.537-12_539del
ENST00000263578.9:c.537-12_539del
ENST00000524751.5:n.473-12_475del
ENST00000525083.5:n.352-412_352-398del
ENST00000525770.5:c.*169-12_*171del
ENST00000526366.5:n.468-12_470del
ENST00000527004.5:c.534-412_534-398del	ENSP00000436374.1:n.534-412_534-398del
ENST00000527875.1:n.367-12_369del
ENST00000530642.1:n.1002_1016del
ENST00000532101.5:n.760-12_762del
ENST00000532125.1:c.495-12_497del
ENST00000533395.5:n.365-412_365-398del
ENST00000533839.5:n.238-879_238-865del
ENST00000534011.5:n.593-16_593-2del
ENST00000534315.5:n.944-412_944-398del
NM_017547.3:c.537-12_539del
NR_037647.1:n.483-12_485del
NR_037648.1:n.723-12_725del
XM_006718879.2:c.27-12_29del
XM_006718880.2:c.-2-412_-2-398del	XP_006718943.1:n.-2-412_-2-398del
XM_006718881.2:c.-2-412_-2-398del	XP_006718944.1:n.-2-412_-2-398del
XM_011542895.1:c.27-12_29del
XM_011542896.1:c.27-12_29del
XM_006718879.3:c.27-12_29del
XM_006718881.3:c.-2-412_-2-398del	XP_006718944.1:n.-2-412_-2-398del
XM_011542895.2:c.27-12_29del
XM_011542896.2:c.27-12_29del
XM_017018000.2:c.537-12_539del
XM_017018001.1:c.27-12_29del
XM_017018002.1:c.27-12_29del
XM_017018003.2:c.-2-412_-2-398del	XP_016873492.1:n.-2-412_-2-398del
XM_017018004.1:c.-2-412_-2-398del	XP_016873493.1:n.-2-412_-2-398del
XM_017018005.1:c.-2-412_-2-398del	XP_016873494.1:n.-2-412_-2-398del
XM_017018006.2:c.-2-412_-2-398del	XP_016873495.1:n.-2-412_-2-398del
NM_017547.4:c.537-12_539del
NR_037647.2:n.369-12_371del
NR_037648.2:n.714-12_716del