Canonical Allele Identifier: CA383229919

Gene: FOXRED1

Linked Data

• gnomAD v4: 11-126274958-C-G
• MyVariant Identifiers: chr11:g.126144853C>G (hg19) ; chr11:g.126274958C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.126274958C>G , CM000673.2:g.126274958C>G	GRCh38
NC_000011.9:g.126144853C>G , CM000673.1:g.126144853C>G	GRCh37
NC_000011.8:g.125650063C>G	NCBI36
NG_028029.1:g.10919C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525083.6:n.746C>G
ENST00000532101.6:n.734-369C>G
ENST00000532125.2:c.565C>G	ENSP00000434178.2:p.Pro189Ala
ENST00000533839.6:c.86-836C>G	ENSP00000509952.1:n.86-836C>G
ENST00000534011.6:n.860C>G
ENST00000685484.1:c.568C>G	ENSP00000510622.1:p.Pro190Ala
ENST00000685601.1:c.568C>G	ENSP00000510603.1:p.Pro190Ala
ENST00000685765.1:c.568C>G	ENSP00000509991.1:p.Pro190Ala
ENST00000685844.1:c.*169-369C>G	ENSP00000509820.1:n.*169-369C>G
ENST00000685857.1:n.1002C>G
ENST00000686242.1:c.367C>G	ENSP00000508950.1:n.367C>G
ENST00000686888.1:c.*135C>G	ENSP00000509619.1:n.*135C>G
ENST00000687699.1:c.692C>G	ENSP00000508878.1:n.692C>G
ENST00000687786.1:n.2068-369C>G
ENST00000688100.1:n.1489C>G
ENST00000688588.1:c.568C>G	ENSP00000510802.1:p.Pro190Ala
ENST00000688927.1:n.2474C>G
ENST00000689283.1:c.*231C>G	ENSP00000509050.1:n.*231C>G
ENST00000689477.1:c.*461C>G	ENSP00000508945.1:n.*461C>G
ENST00000689765.1:c.*169-413C>G	ENSP00000509625.1:n.*169-413C>G
ENST00000690512.1:c.*419C>G	ENSP00000509793.1:n.*419C>G
ENST00000692039.1:c.*366C>G	ENSP00000508821.1:n.*366C>G
ENST00000692336.1:c.592C>G	ENSP00000508540.1:p.Pro198Ala
ENST00000693133.1:n.743C>G
ENST00000263578.10:c.568C>G MANE Select	ENSP00000263578.5:p.Pro190Ala
ENST00000263578.9:c.568C>G	ENSP00000263578.5:p.Pro190Ala
ENST00000524751.5:n.504C>G
ENST00000525083.5:n.352-369C>G
ENST00000525770.5:c.*200C>G	ENSP00000434739.1:n.*200C>G
ENST00000526366.5:n.499C>G
ENST00000527004.5:c.534-369C>G	ENSP00000436374.1:n.534-369C>G
ENST00000527875.1:n.398C>G
ENST00000530642.1:n.1045C>G
ENST00000532101.5:n.791C>G
ENST00000532125.1:c.526C>G	ENSP00000434178.1:p.Pro176Ala
ENST00000533395.5:n.365-369C>G
ENST00000533839.5:n.238-836C>G
ENST00000534011.5:n.620C>G
ENST00000534315.5:n.944-369C>G
NM_017547.3:c.568C>G	NP_060017.1:p.Pro190Ala
NR_037647.1:n.514C>G
NR_037648.1:n.754C>G
XM_006718879.2:c.58C>G	XP_006718942.1:p.Pro20Ala
XM_006718880.2:c.-2-369C>G	XP_006718943.1:n.-2-369C>G
XM_006718881.2:c.-2-369C>G	XP_006718944.1:n.-2-369C>G
XM_011542895.1:c.58C>G	XP_011541197.1:p.Pro20Ala
XM_011542896.1:c.58C>G	XP_011541198.1:p.Pro20Ala
XM_006718879.3:c.58C>G	XP_006718942.1:p.Pro20Ala
XM_006718881.3:c.-2-369C>G	XP_006718944.1:n.-2-369C>G
XM_011542895.2:c.58C>G	XP_011541197.1:p.Pro20Ala
XM_011542896.2:c.58C>G	XP_011541198.1:p.Pro20Ala
XM_017018000.2:c.568C>G	XP_016873489.1:p.Pro190Ala
XM_017018001.1:c.58C>G	XP_016873490.1:p.Pro20Ala
XM_017018002.1:c.58C>G	XP_016873491.1:p.Pro20Ala
XM_017018003.2:c.-2-369C>G	XP_016873492.1:n.-2-369C>G
XM_017018004.1:c.-2-369C>G	XP_016873493.1:n.-2-369C>G
XM_017018005.1:c.-2-369C>G	XP_016873494.1:n.-2-369C>G
XM_017018006.2:c.-2-369C>G	XP_016873495.1:n.-2-369C>G
NM_017547.4:c.568C>G MANE Select	NP_060017.1:p.Pro190Ala
NR_037647.2:n.400C>G
NR_037648.2:n.745C>G