Canonical Allele Identifier: CA9584799

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49828422del , CM000681.2:g.49828422del	GRCh38
NC_000019.9:g.50331679del , CM000681.1:g.50331679del	GRCh37
NC_000019.8:g.55023491del	NCBI36
NG_017091.1:g.15144del , LRG_368:g.15144del

Transcript Alleles

HGVS	Amino-acid Change
NM_030973.4:c.306-27del MANE Select	NP_112235.2:n.306-27del
ENST00000312865.10:c.306-27del MANE Select	ENSP00000326767.5:n.306-27del
NM_001378355.1:c.306-27del	NP_001365284.1:n.306-27del
NM_030973.3:c.306-27del , LRG_368t1:c.306-27del	NP_112235.2:n.306-27del
ENST00000538643.5:c.181-2089del	ENSP00000437496.1:n.181-2089del
ENST00000593767.3:c.306-27del	ENSP00000470692.3:n.306-27del
ENST00000595185.5:c.306-27del	ENSP00000470027.1:n.306-27del
ENST00000612791.4:c.306-27del	ENSP00000479851.1:n.306-27del
ENST00000612854.4:c.306-27del	ENSP00000482155.1:n.306-27del
ENST00000617849.4:c.158-2317del	ENSP00000484882.1:n.158-2317del
ENST00000618715.4:c.158-2316del	ENSP00000480731.1:n.158-2316del
ENST00000620467.4:c.306-27del	ENSP00000482659.1:n.306-27del
ENST00000622402.4:c.146-7405del	ENSP00000478074.1:n.146-7405del
XM_011527353.1:c.306-27del	XP_011525655.1:n.306-27del