Canonical Allele Identifier: CA2340605259

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830634G= , CM000681.2:g.49830634G=	GRCh38
NC_000019.9:g.50333891G= , CM000681.1:g.50333891G=	GRCh37
NC_000019.8:g.55025703G=	NCBI36
NG_017091.1:g.17356G= , LRG_368:g.17356G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.907+36G=	ENSP00000470692.3:n.907+36G=
ENST00000312865.10:c.907+36G= MANE Select	ENSP00000326767.5:n.907+36G=
ENST00000538643.5:c.268+36G=	ENSP00000437496.1:n.268+36G=
ENST00000595185.5:c.688+686G=	ENSP00000470027.1:n.688+686G=
ENST00000612791.4:c.761+472G=	ENSP00000479851.1:n.761+472G=
ENST00000612854.4:c.450+1619G=	ENSP00000482155.1:n.450+1619G=
ENST00000617849.4:c.158-105G=	ENSP00000484882.1:n.158-105G=
ENST00000618715.4:c.158-104G=	ENSP00000480731.1:n.158-104G=
ENST00000620467.4:c.907+36G=	ENSP00000482659.1:n.907+36G=
ENST00000622402.4:c.146-5193G=	ENSP00000478074.1:n.146-5193G=
NM_030973.3:c.907+36G= , LRG_368t1:c.907+36G=	NP_112235.2:n.907+36G=
XM_011527353.1:c.907+36G=	XP_011525655.1:n.907+36G=
NM_001378355.1:c.907+36G=	NP_001365284.1:n.907+36G=
NM_030973.4:c.907+36G= MANE Select	NP_112235.2:n.907+36G=