Canonical Allele Identifier: CA2340604901

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829944G= , CM000681.2:g.49829944G=	GRCh38
NC_000019.9:g.50333201G= , CM000681.1:g.50333201G=	GRCh37
NC_000019.8:g.55025013G=	NCBI36
NG_017091.1:g.16666G= , LRG_368:g.16666G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.684G=	ENSP00000470692.3:p.Leu228=
ENST00000312865.10:c.684G= MANE Select	ENSP00000326767.5:p.Leu228=
ENST00000538643.5:c.181-567G=	ENSP00000437496.1:n.181-567G=
ENST00000595185.5:c.684G=	ENSP00000470027.1:p.Leu228=
ENST00000612791.4:c.682G=	ENSP00000479851.1:p.Ala228=
ENST00000612854.4:c.450+929G=	ENSP00000482155.1:n.450+929G=
ENST00000617849.4:c.158-795G=	ENSP00000484882.1:n.158-795G=
ENST00000618715.4:c.158-794G=	ENSP00000480731.1:n.158-794G=
ENST00000620467.4:c.684G=	ENSP00000482659.1:p.Leu228=
ENST00000622402.4:c.146-5883G=	ENSP00000478074.1:n.146-5883G=
NM_030973.3:c.684G= , LRG_368t1:c.684G=	NP_112235.2:p.Leu228=
XM_011527353.1:c.684G=	XP_011525655.1:p.Leu228=
NM_001378355.1:c.684G=	NP_001365284.1:p.Leu228=
NM_030973.4:c.684G= MANE Select	NP_112235.2:p.Leu228=