Canonical Allele Identifier: CA2275227458
Community Standard Title: NM_024417.5(FDXR):c.1429G= (p.Glu477=)
Gene: FDXR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74862864C= , CM000679.2:g.74862864C= GRCh38
NC_000017.10:g.72858986C= , CM000679.1:g.72858986C= GRCh37
NC_000017.9:g.70370581C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_024417.5:c.1429G= MANE Select NP_077728.3:p.Glu477=
ENST00000293195.10:c.1429G= MANE Select ENSP00000293195.5:p.Glu477=
NM_001258012.3:c.1558G= NP_001244941.2:p.Glu520=
NM_001258012.4:c.1558G= NP_001244941.2:p.Glu520=
NM_001258013.3:c.1522G= NP_001244942.2:p.Glu508=
NM_001258013.4:c.1522G= NP_001244942.2:p.Glu508=
NM_001258014.3:c.1405G= NP_001244943.2:p.Glu469=
NM_001258014.4:c.1405G= NP_001244943.2:p.Glu469=
NM_001258015.2:c.1309G= NP_001244944.1:p.Glu437=
NM_001258015.3:c.1309G= NP_001244944.1:p.Glu437=
NM_001258016.3:c.1273G= NP_001244945.2:p.Glu425=
NM_004110.5:c.1447G= NP_004101.3:p.Glu483=
NM_004110.6:c.1447G= NP_004101.3:p.Glu483=
NM_024417.4:c.1429G= NP_077728.3:p.Glu477=
NR_047576.2:n.1616G=
NR_047576.3:n.1579G=
ENST00000293195.9:c.1429G= ENSP00000293195.5:p.Glu477=
ENST00000413947.6:c.1522G= ENSP00000408595.2:p.Glu508=
ENST00000420580.6:c.1309G= ENSP00000414172.2:p.Glu437=
ENST00000442102.6:c.1558G= ENSP00000416515.2:p.Glu520=
ENST00000544854.5:c.1273G= ENSP00000445432.1:p.Glu425=
ENST00000577509.5:c.*1388G= ENSP00000462083.1:n.*1388G=
ENST00000578473.5:n.2117G=
ENST00000579482.5:c.*1621G= ENSP00000461993.1:n.*1621G=
ENST00000581530.5:c.1447G= ENSP00000462972.1:p.Glu483=
ENST00000582944.5:c.1405G= ENSP00000462183.1:p.Glu469=
ENST00000583881.5:c.*894G= ENSP00000464670.1:n.*894G=
ENST00000583917.5:c.1345G= ENSP00000463940.1:p.Glu449=
XM_006721772.1:c.1432G= XP_006721835.1:p.Glu478=
XM_006721772.2:c.1432G= XP_006721835.1:p.Glu478=
XM_011524527.1:c.1450G= XP_011522829.1:p.Glu484=
XM_011524527.2:c.1450G= XP_011522829.1:p.Glu484=
XM_011524528.1:c.1441G= XP_011522830.1:p.Glu481=
XM_011524529.1:c.1438G= XP_011522831.1:p.Glu480=
XM_011524530.1:c.1312G= XP_011522832.1:p.Glu438=
XM_011524531.1:c.1294G= XP_011522833.1:p.Glu432=
XM_011524531.2:c.1294G= XP_011522833.1:p.Glu432=
XM_011524532.1:c.1291G= XP_011522834.1:p.Glu431=
XM_011524532.2:c.1291G= XP_011522834.1:p.Glu431=
XM_011524533.1:c.1276G= XP_011522835.1:p.Glu426=
XM_011524533.2:c.1276G= XP_011522835.1:p.Glu426=
XM_024450648.1:c.1147G= XP_024306416.1:p.Glu383=
XM_024450649.1:c.700G= XP_024306417.1:p.Glu234=
XM_024450650.1:c.700G= XP_024306418.1:p.Glu234=
XR_002957983.1:n.2285G=