Canonical Allele Identifier: CA354959160
Gene: MED12L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.151165846G>A , CM000665.2:g.151165846G>A GRCh38
NC_000003.11:g.150883633G>A , CM000665.1:g.150883633G>A GRCh37
NC_000003.10:g.152366323G>A NCBI36
NG_021244.1:g.83958G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001393769.1:c.1358G>A MANE Select NP_001380698.1:p.Gly453Glu
ENST00000687756.1:c.1358G>A MANE Select ENSP00000508695.1:p.Gly453Glu
NM_053002.5:c.1358G>A NP_443728.3:p.Gly453Glu
NM_053002.6:c.1358G>A NP_443728.3:p.Gly453Glu
ENST00000273432.8:c.938G>A ENSP00000273432.4:p.Gly313Glu
ENST00000309237.8:c.1358G>A ENSP00000310760.4:p.Gly453Glu
ENST00000422248.6:c.1358G>A ENSP00000403308.2:p.Gly453Glu
ENST00000474524.5:c.1358G>A ENSP00000417235.1:p.Gly453Glu
ENST00000685357.1:n.1616G>A
ENST00000686666.1:c.1253G>A ENSP00000509482.1:p.Gly418Glu
ENST00000688234.1:c.1358G>A ENSP00000509197.1:p.Gly453Glu
ENST00000693531.1:n.1433G>A
XM_006713487.2:c.1358G>A XP_006713550.1:p.Gly453Glu
XM_006713487.3:c.1358G>A XP_006713550.1:p.Gly453Glu
XM_011512386.1:c.1358G>A XP_011510688.1:p.Gly453Glu
XM_011512387.1:c.1358G>A XP_011510689.1:p.Gly453Glu
XM_011512388.1:c.1358G>A XP_011510690.1:p.Gly453Glu
XM_011512389.1:c.1358G>A XP_011510691.1:p.Gly453Glu
XM_011512390.1:c.1358G>A XP_011510692.1:p.Gly453Glu
XM_011512390.2:c.1358G>A XP_011510692.1:p.Gly453Glu
XM_011512391.1:c.1088G>A XP_011510693.1:p.Gly363Glu
XM_011512392.1:c.902G>A XP_011510694.1:p.Gly301Glu
XM_011512393.1:c.1358G>A XP_011510695.1:p.Gly453Glu
XM_011512394.1:c.1358G>A XP_011510696.1:p.Gly453Glu
XM_011512394.2:c.1358G>A XP_011510696.1:p.Gly453Glu
XM_011512395.1:c.1358G>A XP_011510697.1:p.Gly453Glu
XM_011512399.1:c.1358G>A XP_011510701.1:p.Gly453Glu
XM_011512399.3:c.1358G>A XP_011510701.1:p.Gly453Glu
XM_017005676.1:c.1358G>A XP_016861165.1:p.Gly453Glu
XM_017005677.1:c.1358G>A XP_016861166.1:p.Gly453Glu
XM_017005678.1:c.1358G>A XP_016861167.1:p.Gly453Glu
XM_017005679.1:c.1088G>A XP_016861168.1:p.Gly363Glu
XM_017005680.1:c.1358G>A XP_016861169.1:p.Gly453Glu
XR_001740000.1:n.1759G>A