Canonical Allele Identifier: CA406919981

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49835779G>A , CM000681.2:g.49835779G>A	GRCh38
NC_000019.9:g.50339036G>A , CM000681.1:g.50339036G>A	GRCh37
NC_000019.8:g.55030848G>A	NCBI36
NG_017091.1:g.22501G>A , LRG_368:g.22501G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.1799G>A	ENSP00000470692.3:p.Gly600Glu
ENST00000312865.10:c.1799G>A MANE Select	ENSP00000326767.5:p.Gly600Glu
ENST00000538643.5:c.1160G>A	ENSP00000437496.1:p.Gly387Glu
ENST00000593767.1:c.245G>A
ENST00000594998.1:n.2419G>A
ENST00000595185.5:c.689-1112G>A	ENSP00000470027.1:n.689-1112G>A
ENST00000612791.4:c.762-1060G>A	ENSP00000479851.1:n.762-1060G>A
ENST00000612854.4:c.451-474G>A	ENSP00000482155.1:n.451-474G>A
ENST00000617849.4:c.1004G>A	ENSP00000484882.1:p.Gly335Glu
ENST00000618715.4:c.1004G>A	ENSP00000480731.1:p.Gly335Glu
ENST00000620467.4:c.973-504G>A	ENSP00000482659.1:n.973-504G>A
ENST00000622046.1:c.266G>A	ENSP00000483584.1:p.Gly89Glu
ENST00000622402.4:c.146-48G>A	ENSP00000478074.1:n.146-48G>A
NM_030973.3:c.1799G>A , LRG_368t1:c.1799G>A	NP_112235.2:p.Gly600Glu
XM_011527353.1:c.1799G>A	XP_011525655.1:p.Gly600Glu
NM_001378355.1:c.1799G>A	NP_001365284.1:p.Gly600Glu
NM_030973.4:c.1799G>A MANE Select	NP_112235.2:p.Gly600Glu