Canonical Allele Identifier: CA2340604902

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829947T= , CM000681.2:g.49829947T=	GRCh38
NC_000019.9:g.50333204T= , CM000681.1:g.50333204T=	GRCh37
NC_000019.8:g.55025016T=	NCBI36
NG_017091.1:g.16669T= , LRG_368:g.16669T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.687T=	ENSP00000470692.3:p.Pro229=
ENST00000312865.10:c.687T= MANE Select	ENSP00000326767.5:p.Pro229=
ENST00000538643.5:c.181-564T=	ENSP00000437496.1:n.181-564T=
ENST00000595185.5:c.687T=	ENSP00000470027.1:p.Pro229=
ENST00000612791.4:c.685T=	ENSP00000479851.1:p.Cys229=
ENST00000612854.4:c.450+932T=	ENSP00000482155.1:n.450+932T=
ENST00000617849.4:c.158-792T=	ENSP00000484882.1:n.158-792T=
ENST00000618715.4:c.158-791T=	ENSP00000480731.1:n.158-791T=
ENST00000620467.4:c.687T=	ENSP00000482659.1:p.Pro229=
ENST00000622402.4:c.146-5880T=	ENSP00000478074.1:n.146-5880T=
NM_030973.3:c.687T= , LRG_368t1:c.687T=	NP_112235.2:p.Pro229=
XM_011527353.1:c.687T=	XP_011525655.1:p.Pro229=
NM_001378355.1:c.687T=	NP_001365284.1:p.Pro229=
NM_030973.4:c.687T= MANE Select	NP_112235.2:p.Pro229=