Canonical Allele Identifier: CA2340604863

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829869G= , CM000681.2:g.49829869G=	GRCh38
NC_000019.9:g.50333126G= , CM000681.1:g.50333126G=	GRCh37
NC_000019.8:g.55024938G=	NCBI36
NG_017091.1:g.16591G= , LRG_368:g.16591G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.609G=	ENSP00000470692.3:p.Leu203=
ENST00000312865.10:c.609G= MANE Select	ENSP00000326767.5:p.Leu203=
ENST00000538643.5:c.181-642G=	ENSP00000437496.1:n.181-642G=
ENST00000595185.5:c.609G=	ENSP00000470027.1:p.Leu203=
ENST00000612791.4:c.607G=	ENSP00000479851.1:p.Ala203=
ENST00000612854.4:c.450+854G=	ENSP00000482155.1:n.450+854G=
ENST00000617849.4:c.158-870G=	ENSP00000484882.1:n.158-870G=
ENST00000618715.4:c.158-869G=	ENSP00000480731.1:n.158-869G=
ENST00000620467.4:c.609G=	ENSP00000482659.1:p.Leu203=
ENST00000622402.4:c.146-5958G=	ENSP00000478074.1:n.146-5958G=
NM_030973.3:c.609G= , LRG_368t1:c.609G=	NP_112235.2:p.Leu203=
XM_011527353.1:c.609G=	XP_011525655.1:p.Leu203=
NM_001378355.1:c.609G=	NP_001365284.1:p.Leu203=
NM_030973.4:c.609G= MANE Select	NP_112235.2:p.Leu203=