Canonical Allele Identifier: CA338259

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49835774C>T , CM000681.2:g.49835774C>T	GRCh38
NC_000019.9:g.50339031C>T , CM000681.1:g.50339031C>T	GRCh37
NC_000019.8:g.55030843C>T	NCBI36
NG_017091.1:g.22496C>T , LRG_368:g.22496C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.1794C>T	ENSP00000470692.3:p.Ala598=
ENST00000312865.10:c.1794C>T MANE Select	ENSP00000326767.5:p.Ala598=
ENST00000538643.5:c.1155C>T	ENSP00000437496.1:p.Ala385=
ENST00000593767.1:c.240C>T
ENST00000594998.1:n.2414C>T
ENST00000595185.5:c.689-1117C>T	ENSP00000470027.1:n.689-1117C>T
ENST00000612791.4:c.762-1065C>T	ENSP00000479851.1:n.762-1065C>T
ENST00000612854.4:c.451-479C>T	ENSP00000482155.1:n.451-479C>T
ENST00000617849.4:c.999C>T	ENSP00000484882.1:p.Ala333=
ENST00000618715.4:c.999C>T	ENSP00000480731.1:p.Ala333=
ENST00000620467.4:c.973-509C>T	ENSP00000482659.1:n.973-509C>T
ENST00000622046.1:c.261C>T	ENSP00000483584.1:p.Ala87=
ENST00000622402.4:c.146-53C>T	ENSP00000478074.1:n.146-53C>T
NM_030973.3:c.1794C>T , LRG_368t1:c.1794C>T	NP_112235.2:p.Ala598=
XM_011527353.1:c.1794C>T	XP_011525655.1:p.Ala598=
NM_001378355.1:c.1794C>T	NP_001365284.1:p.Ala598=
NM_030973.4:c.1794C>T MANE Select	NP_112235.2:p.Ala598=