Canonical Allele Identifier: CA508295407

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49835879C>T , CM000681.2:g.49835879C>T	GRCh38
NC_000019.9:g.50339136C>T , CM000681.1:g.50339136C>T	GRCh37
NC_000019.8:g.55030948C>T	NCBI36
NG_017091.1:g.22601C>T , LRG_368:g.22601C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.1899C>T	ENSP00000470692.3:p.Pro633=
ENST00000312865.10:c.1899C>T MANE Select	ENSP00000326767.5:p.Pro633=
ENST00000538643.5:c.1260C>T	ENSP00000437496.1:p.Pro420=
ENST00000593767.1:c.345C>T
ENST00000594998.1:n.2519C>T
ENST00000595185.5:c.689-1012C>T	ENSP00000470027.1:n.689-1012C>T
ENST00000612791.4:c.762-960C>T	ENSP00000479851.1:n.762-960C>T
ENST00000612854.4:c.451-374C>T	ENSP00000482155.1:n.451-374C>T
ENST00000617849.4:c.1104C>T	ENSP00000484882.1:p.Pro368=
ENST00000618715.4:c.1104C>T	ENSP00000480731.1:p.Pro368=
ENST00000620467.4:c.973-404C>T	ENSP00000482659.1:n.973-404C>T
ENST00000622046.1:c.366C>T	ENSP00000483584.1:p.Pro122=
ENST00000622402.4:c.198C>T	ENSP00000478074.1:p.Pro66=
NM_030973.3:c.1899C>T , LRG_368t1:c.1899C>T	NP_112235.2:p.Pro633=
XM_011527353.1:c.1899C>T	XP_011525655.1:p.Pro633=
NM_001378355.1:c.1899C>T	NP_001365284.1:p.Pro633=
NM_030973.4:c.1899C>T MANE Select	NP_112235.2:p.Pro633=