Canonical Allele Identifier: CA2340607492

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49834979C= , CM000681.2:g.49834979C=	GRCh38
NC_000019.9:g.50338236C= , CM000681.1:g.50338236C=	GRCh37
NC_000019.8:g.55030048C=	NCBI36
NG_017091.1:g.21701C= , LRG_368:g.21701C=

Transcript Alleles

HGVS	Amino-acid Change
NM_030973.4:c.1483-7C= MANE Select	NP_112235.2:n.1483-7C=
ENST00000312865.10:c.1483-7C= MANE Select	ENSP00000326767.5:n.1483-7C=
NM_001378355.1:c.1483-7C=	NP_001365284.1:n.1483-7C=
NM_030973.3:c.1483-7C= , LRG_368t1:c.1483-7C=	NP_112235.2:n.1483-7C=
ENST00000538643.5:c.844-7C=	ENSP00000437496.1:n.844-7C=
ENST00000593767.3:c.1483-7C=	ENSP00000470692.3:n.1483-7C=
ENST00000594998.1:n.2096C=
ENST00000595185.5:c.689-1912C=	ENSP00000470027.1:n.689-1912C=
ENST00000612791.4:c.762-1860C=	ENSP00000479851.1:n.762-1860C=
ENST00000612854.4:c.451-1274C=	ENSP00000482155.1:n.451-1274C=
ENST00000617849.4:c.688-7C=	ENSP00000484882.1:n.688-7C=
ENST00000618715.4:c.688-7C=	ENSP00000480731.1:n.688-7C=
ENST00000620467.4:c.973-1304C=	ENSP00000482659.1:n.973-1304C=
ENST00000622046.1:c.-58C=	ENSP00000483584.1:n.-58C=
ENST00000622402.4:c.146-848C=	ENSP00000478074.1:n.146-848C=
XM_011527353.1:c.1483-7C=	XP_011525655.1:n.1483-7C=