Canonical Allele Identifier: CA673003897

Gene: FOXRED1

Linked Data

• dbSNP Id: rs1343670962
• MyVariant Identifiers: chr11:g.126145370_126145371del (hg19) ; chr11:g.126275475_126275476del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275475_126275476del , CM000673.2:g.126275475_126275476del	GRCh38
NC_000011.9:g.126145370_126145371del , CM000673.1:g.126145370_126145371del	GRCh37
NC_000011.8:g.125650580_125650581del	NCBI36
NG_028029.1:g.11436_11437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1216+47_1216+48del
ENST00000532101.6:n.835+47_835+48del
ENST00000532125.2:c.730+47_730+48del	ENSP00000434178.2:n.730+47_730+48del
ENST00000533839.6:c.86-319_86-318del	ENSP00000509952.1:n.86-319_86-318del
ENST00000534011.6:n.1025+47_1025+48del
ENST00000685484.1:c.733+47_733+48del	ENSP00000510622.1:n.733+47_733+48del
ENST00000685601.1:c.733+47_733+48del	ENSP00000510603.1:n.733+47_733+48del
ENST00000685765.1:c.733+47_733+48del	ENSP00000509991.1:n.733+47_733+48del
ENST00000685844.1:c.*270+47_*270+48del	ENSP00000509820.1:n.*270+47_*270+48del
ENST00000685857.1:n.1519_1520del
ENST00000686242.1:c.532+47_532+48del	ENSP00000508950.1:n.532+47_532+48del
ENST00000686888.1:c.*300+47_*300+48del	ENSP00000509619.1:n.*300+47_*300+48del
ENST00000687699.1:c.857+47_857+48del	ENSP00000508878.1:n.857+47_857+48del
ENST00000687786.1:n.2169+47_2169+48del
ENST00000688100.1:n.1654+47_1654+48del
ENST00000688588.1:c.733+47_733+48del	ENSP00000510802.1:n.733+47_733+48del
ENST00000688927.1:n.2944+47_2944+48del
ENST00000689283.1:c.*396+47_*396+48del	ENSP00000509050.1:n.*396+47_*396+48del
ENST00000689477.1:c.*626+47_*626+48del	ENSP00000508945.1:n.*626+47_*626+48del
ENST00000689765.1:c.*226+47_*226+48del	ENSP00000509625.1:n.*226+47_*226+48del
ENST00000690512.1:c.*584+47_*584+48del	ENSP00000509793.1:n.*584+47_*584+48del
ENST00000692039.1:c.*531+47_*531+48del	ENSP00000508821.1:n.*531+47_*531+48del
ENST00000692336.1:c.757+47_757+48del	ENSP00000508540.1:n.757+47_757+48del
ENST00000693133.1:n.1260_1261del
ENST00000263578.10:c.733+47_733+48del MANE Select	ENSP00000263578.5:n.733+47_733+48del
ENST00000263578.9:c.733+47_733+48del	ENSP00000263578.5:n.733+47_733+48del
ENST00000525083.5:n.453+47_453+48del
ENST00000525770.5:c.*365+47_*365+48del	ENSP00000434739.1:n.*365+47_*365+48del
ENST00000527004.5:c.*77+47_*77+48del	ENSP00000436374.1:n.*77+47_*77+48del
ENST00000530642.1:n.1562_1563del
ENST00000532101.5:n.956+47_956+48del
ENST00000532125.1:c.691+47_691+48del	ENSP00000434178.1:n.691+47_691+48del
ENST00000533395.5:n.466+47_466+48del
ENST00000533839.5:n.238-319_238-318del
ENST00000534011.5:n.785+47_785+48del
ENST00000534315.5:n.1045+47_1045+48del
NM_017547.3:c.733+47_733+48del	NP_060017.1:n.733+47_733+48del
NR_037647.1:n.679+47_679+48del
NR_037648.1:n.919+47_919+48del
XM_006718879.2:c.223+47_223+48del	XP_006718942.1:n.223+47_223+48del
XM_006718880.2:c.100+47_100+48del	XP_006718943.1:n.100+47_100+48del
XM_006718881.2:c.100+47_100+48del	XP_006718944.1:n.100+47_100+48del
XM_011542895.1:c.223+47_223+48del	XP_011541197.1:n.223+47_223+48del
XM_011542896.1:c.223+47_223+48del	XP_011541198.1:n.223+47_223+48del
XM_006718879.3:c.223+47_223+48del	XP_006718942.1:n.223+47_223+48del
XM_006718881.3:c.100+47_100+48del	XP_006718944.1:n.100+47_100+48del
XM_011542895.2:c.223+47_223+48del	XP_011541197.1:n.223+47_223+48del
XM_011542896.2:c.223+47_223+48del	XP_011541198.1:n.223+47_223+48del
XM_017018000.2:c.733+47_733+48del	XP_016873489.1:n.733+47_733+48del
XM_017018001.1:c.223+47_223+48del	XP_016873490.1:n.223+47_223+48del
XM_017018002.1:c.223+47_223+48del	XP_016873491.1:n.223+47_223+48del
XM_017018003.2:c.100+47_100+48del	XP_016873492.1:n.100+47_100+48del
XM_017018004.1:c.100+47_100+48del	XP_016873493.1:n.100+47_100+48del
XM_017018005.1:c.100+47_100+48del	XP_016873494.1:n.100+47_100+48del
XM_017018006.2:c.100+47_100+48del	XP_016873495.1:n.100+47_100+48del
NM_017547.4:c.733+47_733+48del MANE Select	NP_060017.1:n.733+47_733+48del
NR_037647.2:n.565+47_565+48del
NR_037648.2:n.910+47_910+48del