Canonical Allele Identifier: CA2340604882

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829908C= , CM000681.2:g.49829908C=	GRCh38
NC_000019.9:g.50333165C= , CM000681.1:g.50333165C=	GRCh37
NC_000019.8:g.55024977C=	NCBI36
NG_017091.1:g.16630C= , LRG_368:g.16630C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.648C=	ENSP00000470692.3:p.Asp216=
ENST00000312865.10:c.648C= MANE Select	ENSP00000326767.5:p.Asp216=
ENST00000538643.5:c.181-603C=	ENSP00000437496.1:n.181-603C=
ENST00000595185.5:c.648C=	ENSP00000470027.1:p.Asp216=
ENST00000612791.4:c.646C=	ENSP00000479851.1:p.Pro216=
ENST00000612854.4:c.450+893C=	ENSP00000482155.1:n.450+893C=
ENST00000617849.4:c.158-831C=	ENSP00000484882.1:n.158-831C=
ENST00000618715.4:c.158-830C=	ENSP00000480731.1:n.158-830C=
ENST00000620467.4:c.648C=	ENSP00000482659.1:p.Asp216=
ENST00000622402.4:c.146-5919C=	ENSP00000478074.1:n.146-5919C=
NM_030973.3:c.648C= , LRG_368t1:c.648C=	NP_112235.2:p.Asp216=
XM_011527353.1:c.648C=	XP_011525655.1:p.Asp216=
NM_001378355.1:c.648C=	NP_001365284.1:p.Asp216=
NM_030973.4:c.648C= MANE Select	NP_112235.2:p.Asp216=