Canonical Allele Identifier: CA8760671
Gene: MIF4GD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.75267839C>A , CM000679.2:g.75267839C>A GRCh38
NC_000017.10:g.73263920C>A , CM000679.1:g.73263920C>A GRCh37
NC_000017.9:g.70775515C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001370592.1:c.255G>T MANE Select NP_001357521.1:p.Gln85His
ENST00000325102.13:c.255G>T MANE Select ENSP00000321625.8:p.Gln85His
NM_001242498.1:c.378G>T NP_001229427.1:p.Gln126His
NM_001242498.2:c.378G>T NP_001229427.1:p.Gln126His
NM_001242500.1:c.357G>T NP_001229429.1:p.Gln119His
NM_001242501.1:c.255G>T NP_001229430.1:p.Gln85His
NM_001363806.1:c.193-209G>T NP_001350735.1:n.193-209G>T
NM_001363806.2:c.193-209G>T NP_001350735.1:n.193-209G>T
NM_001365751.1:c.378G>T NP_001352680.1:p.Gln126His
NM_001365752.1:c.255G>T NP_001352681.1:p.Gln85His
NM_001365753.1:c.255G>T NP_001352682.1:p.Gln85His
NM_001365754.1:c.255G>T NP_001352683.1:p.Gln85His
NM_001365755.1:c.255G>T NP_001352684.1:p.Gln85His
NM_020679.3:c.357G>T NP_065730.2:p.Gln119His
NM_020679.4:c.357G>T NP_065730.2:p.Gln119His
ENST00000245551.9:c.357G>T ENSP00000245551.5:p.Gln119His
ENST00000325102.12:c.255G>T ENSP00000321625.8:p.Gln85His
ENST00000577240.1:n.609G>T
ENST00000577542.5:c.378G>T ENSP00000463334.1:p.Gln126His
ENST00000578305.5:c.83-209G>T ENSP00000463629.1:n.83-209G>T
ENST00000579119.5:c.255G>T ENSP00000463579.1:p.Gln85His
ENST00000579194.5:c.378G>T ENSP00000462655.1:p.Gln126His
ENST00000579194.6:c.378G>T ENSP00000462655.2:p.Gln126His
ENST00000579297.5:c.378G>T ENSP00000462459.1:p.Gln126His
ENST00000579612.5:c.295-209G>T ENSP00000463264.1:n.295-209G>T
ENST00000580571.5:c.193-209G>T ENSP00000462412.1:n.193-209G>T
ENST00000580717.5:c.255G>T ENSP00000464448.1:p.Gln85His
ENST00000581777.1:c.255G>T ENSP00000463493.1:p.Gln85His
ENST00000581777.2:c.459G>T ENSP00000463493.2:p.Gln153His
ENST00000618645.4:c.255G>T ENSP00000484245.1:p.Gln85His
ENST00000618645.5:c.255G>T ENSP00000484245.1:p.Gln85His
ENST00000649805.1:c.378G>T ENSP00000498095.1:p.Gln126His
ENST00000678201.1:n.823G>T
XM_005257530.1:c.378G>T XP_005257587.1:p.Gln126His
XM_005257531.3:c.255G>T XP_005257588.1:p.Gln85His
XM_005257532.3:c.255G>T XP_005257589.1:p.Gln85His
XM_005257532.5:c.255G>T XP_005257589.1:p.Gln85His
XM_005257533.1:c.255G>T XP_005257590.1:p.Gln85His
XM_006721985.2:c.378G>T XP_006722048.1:p.Gln126His
XM_006721986.2:c.378G>T XP_006722049.1:p.Gln126His
XM_011525051.1:c.582G>T XP_011523353.1:p.Gln194His
XM_011525051.2:c.582G>T XP_011523353.1:p.Gln194His
XM_011525052.1:c.561G>T XP_011523354.1:p.Gln187His
XM_011525052.2:c.561G>T XP_011523354.1:p.Gln187His
XM_011525053.1:c.459G>T XP_011523355.1:p.Gln153His
XM_011525053.3:c.459G>T XP_011523355.1:p.Gln153His
XM_011525054.1:c.520-209G>T XP_011523356.1:n.520-209G>T
XM_011525054.2:c.520-209G>T XP_011523356.1:n.520-209G>T
XM_011525055.1:c.397-209G>T XP_011523357.1:n.397-209G>T
XM_011525055.2:c.397-209G>T XP_011523357.1:n.397-209G>T
XM_011525056.1:c.295-209G>T XP_011523358.1:n.295-209G>T
XM_011525057.1:c.193-209G>T XP_011523359.1:n.193-209G>T
XM_011525057.2:c.193-209G>T XP_011523359.1:n.193-209G>T
XM_017024888.1:c.582G>T XP_016880377.1:p.Gln194His
XM_017024889.2:c.378G>T XP_016880378.1:p.Gln126His
XM_017024890.1:c.378G>T XP_016880379.1:p.Gln126His
XM_017024891.2:c.378G>T XP_016880380.1:p.Gln126His
XM_017024895.2:c.295-209G>T XP_016880384.1:n.295-209G>T