Canonical Allele Identifier: CA2340604888

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829918_49829924delinsATGGTGC , CM000681.2:g.49829918_49829924delinsATGGTGC	GRCh38
NC_000019.9:g.50333175_50333181delinsATGGTGC , CM000681.1:g.50333175_50333181delinsATGGTGC	GRCh37
NC_000019.8:g.55024987_55024993delinsATGGTGC	NCBI36
NG_017091.1:g.16640_16646delinsATGGTGC , LRG_368:g.16640_16646delinsATGGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.658_664delinsATGGTGC	ENSP00000470692.3:p.Met220=
ENST00000312865.10:c.658_664delinsATGGTGC MANE Select	ENSP00000326767.5:p.Met220=
ENST00000538643.5:c.181-593_181-587delinsATGGTGC	ENSP00000437496.1:n.181-593_181-587delinsATGGTGC
ENST00000595185.5:c.658_664delinsATGGTGC	ENSP00000470027.1:p.Met220=
ENST00000612791.4:c.656_662delinsATGGTGC	ENSP00000479851.1:p.His219=
ENST00000612854.4:c.450+903_450+909delinsATGGTGC	ENSP00000482155.1:n.450+903_450+909delinsATGGTGC
ENST00000617849.4:c.158-821_158-815delinsATGGTGC	ENSP00000484882.1:n.158-821_158-815delinsATGGTGC
ENST00000618715.4:c.158-820_158-814delinsATGGTGC	ENSP00000480731.1:n.158-820_158-814delinsATGGTGC
ENST00000620467.4:c.658_664delinsATGGTGC	ENSP00000482659.1:p.Met220=
ENST00000622402.4:c.146-5909_146-5903delinsATGGTGC	ENSP00000478074.1:n.146-5909_146-5903delinsATGGTGC
NM_030973.3:c.658_664delinsATGGTGC , LRG_368t1:c.658_664delinsATGGTGC	NP_112235.2:p.Met220=
XM_011527353.1:c.658_664delinsATGGTGC	XP_011525655.1:p.Met220=
NM_001378355.1:c.658_664delinsATGGTGC	NP_001365284.1:p.Met220=
NM_030973.4:c.658_664delinsATGGTGC MANE Select	NP_112235.2:p.Met220=