Canonical Allele Identifier: CA2340605347

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830791C= , CM000681.2:g.49830791C=	GRCh38
NC_000019.9:g.50334048C= , CM000681.1:g.50334048C=	GRCh37
NC_000019.8:g.55025860C=	NCBI36
NG_017091.1:g.17513C= , LRG_368:g.17513C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.1005C=	ENSP00000470692.3:p.Ala335=
ENST00000312865.10:c.1005C= MANE Select	ENSP00000326767.5:p.Ala335=
ENST00000538643.5:c.366C=	ENSP00000437496.1:p.Ala122=
ENST00000595185.5:c.688+843C=	ENSP00000470027.1:n.688+843C=
ENST00000612791.4:c.761+629C=	ENSP00000479851.1:n.761+629C=
ENST00000612854.4:c.450+1776C=	ENSP00000482155.1:n.450+1776C=
ENST00000617849.4:c.210C=	ENSP00000484882.1:p.Ala70=
ENST00000618715.4:c.210C=	ENSP00000480731.1:p.Ala70=
ENST00000620467.4:c.972+33C=	ENSP00000482659.1:n.972+33C=
ENST00000622402.4:c.146-5036C=	ENSP00000478074.1:n.146-5036C=
NM_030973.3:c.1005C= , LRG_368t1:c.1005C=	NP_112235.2:p.Ala335=
XM_011527353.1:c.1005C=	XP_011525655.1:p.Ala335=
NM_001378355.1:c.1005C=	NP_001365284.1:p.Ala335=
NM_030973.4:c.1005C= MANE Select	NP_112235.2:p.Ala335=