Canonical Allele Identifier: CA2340604854

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829855_49829856delinsGC , CM000681.2:g.49829855_49829856delinsGC	GRCh38
NC_000019.9:g.50333112_50333113delinsGC , CM000681.1:g.50333112_50333113delinsGC	GRCh37
NC_000019.8:g.55024924_55024925delinsGC	NCBI36
NG_017091.1:g.16577_16578delinsGC , LRG_368:g.16577_16578delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.595_596delinsGC	ENSP00000470692.3:p.Ala199=
ENST00000312865.10:c.595_596delinsGC MANE Select	ENSP00000326767.5:p.Ala199=
ENST00000538643.5:c.181-656_181-655delinsGC	ENSP00000437496.1:n.181-656_181-655delinsGC
ENST00000595185.5:c.595_596delinsGC	ENSP00000470027.1:p.Ala199=
ENST00000612791.4:c.595_596delinsGC	ENSP00000479851.1:p.Ala199=
ENST00000612854.4:c.450+840_450+841delinsGC	ENSP00000482155.1:n.450+840_450+841delinsGC
ENST00000617849.4:c.158-884_158-883delinsGC	ENSP00000484882.1:n.158-884_158-883delinsGC
ENST00000618715.4:c.158-883_158-882delinsGC	ENSP00000480731.1:n.158-883_158-882delinsGC
ENST00000620467.4:c.595_596delinsGC	ENSP00000482659.1:p.Ala199=
ENST00000622402.4:c.146-5972_146-5971delinsGC	ENSP00000478074.1:n.146-5972_146-5971delinsGC
NM_030973.3:c.595_596delinsGC , LRG_368t1:c.595_596delinsGC	NP_112235.2:p.Ala199=
XM_011527353.1:c.595_596delinsGC	XP_011525655.1:p.Ala199=
NM_001378355.1:c.595_596delinsGC	NP_001365284.1:p.Ala199=
NM_030973.4:c.595_596delinsGC MANE Select	NP_112235.2:p.Ala199=