Canonical Allele Identifier: CA383230111

Gene: FOXRED1

Linked Data

• MyVariant Identifiers: chr11:g.126145240G>C (hg19) ; chr11:g.126275345G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126275345G>C , CM000673.2:g.126275345G>C	GRCh38
NC_000011.9:g.126145240G>C , CM000673.1:g.126145240G>C	GRCh37
NC_000011.8:g.125650450G>C	NCBI36
NG_028029.1:g.11306G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.1133G>C
ENST00000532101.6:n.752G>C
ENST00000532125.2:c.647G>C	ENSP00000434178.2:p.Trp216Ser
ENST00000533839.6:c.86-449G>C	ENSP00000509952.1:n.86-449G>C
ENST00000534011.6:n.942G>C
ENST00000685484.1:c.650G>C	ENSP00000510622.1:p.Trp217Ser
ENST00000685601.1:c.650G>C	ENSP00000510603.1:p.Trp217Ser
ENST00000685765.1:c.650G>C	ENSP00000509991.1:p.Trp217Ser
ENST00000685844.1:c.*187G>C	ENSP00000509820.1:n.*187G>C
ENST00000685857.1:n.1389G>C
ENST00000686242.1:c.449G>C	ENSP00000508950.1:n.449G>C
ENST00000686888.1:c.*217G>C	ENSP00000509619.1:n.*217G>C
ENST00000687699.1:c.774G>C	ENSP00000508878.1:n.774G>C
ENST00000687786.1:n.2086G>C
ENST00000688100.1:n.1571G>C
ENST00000688588.1:c.650G>C	ENSP00000510802.1:p.Trp217Ser
ENST00000688927.1:n.2861G>C
ENST00000689283.1:c.*313G>C	ENSP00000509050.1:n.*313G>C
ENST00000689477.1:c.*543G>C	ENSP00000508945.1:n.*543G>C
ENST00000689765.1:c.*169-26G>C	ENSP00000509625.1:n.*169-26G>C
ENST00000690512.1:c.*501G>C	ENSP00000509793.1:n.*501G>C
ENST00000692039.1:c.*448G>C	ENSP00000508821.1:n.*448G>C
ENST00000692336.1:c.674G>C	ENSP00000508540.1:p.Trp225Ser
ENST00000693133.1:n.1130G>C
ENST00000263578.10:c.650G>C MANE Select	ENSP00000263578.5:p.Trp217Ser
ENST00000263578.9:c.650G>C	ENSP00000263578.5:p.Trp217Ser
ENST00000524751.5:n.891G>C
ENST00000525083.5:n.370G>C
ENST00000525770.5:c.*282G>C	ENSP00000434739.1:n.*282G>C
ENST00000527004.5:c.552G>C	ENSP00000436374.1:p.Leu184Phe
ENST00000530642.1:n.1432G>C
ENST00000532101.5:n.873G>C
ENST00000532125.1:c.608G>C	ENSP00000434178.1:p.Trp203Ser
ENST00000533395.5:n.383G>C
ENST00000533839.5:n.238-449G>C
ENST00000534011.5:n.702G>C
ENST00000534315.5:n.962G>C
NM_017547.3:c.650G>C	NP_060017.1:p.Trp217Ser
NR_037647.1:n.596G>C
NR_037648.1:n.836G>C
XM_006718879.2:c.140G>C	XP_006718942.1:p.Trp47Ser
XM_006718880.2:c.17G>C	XP_006718943.1:p.Trp6Ser
XM_006718881.2:c.17G>C	XP_006718944.1:p.Trp6Ser
XM_011542895.1:c.140G>C	XP_011541197.1:p.Trp47Ser
XM_011542896.1:c.140G>C	XP_011541198.1:p.Trp47Ser
XM_006718879.3:c.140G>C	XP_006718942.1:p.Trp47Ser
XM_006718881.3:c.17G>C	XP_006718944.1:p.Trp6Ser
XM_011542895.2:c.140G>C	XP_011541197.1:p.Trp47Ser
XM_011542896.2:c.140G>C	XP_011541198.1:p.Trp47Ser
XM_017018000.2:c.650G>C	XP_016873489.1:p.Trp217Ser
XM_017018001.1:c.140G>C	XP_016873490.1:p.Trp47Ser
XM_017018002.1:c.140G>C	XP_016873491.1:p.Trp47Ser
XM_017018003.2:c.17G>C	XP_016873492.1:p.Trp6Ser
XM_017018004.1:c.17G>C	XP_016873493.1:p.Trp6Ser
XM_017018005.1:c.17G>C	XP_016873494.1:p.Trp6Ser
XM_017018006.2:c.17G>C	XP_016873495.1:p.Trp6Ser
NM_017547.4:c.650G>C MANE Select	NP_060017.1:p.Trp217Ser
NR_037647.2:n.482G>C
NR_037648.2:n.827G>C