Canonical Allele Identifier: CA406913082

Gene: MED25

Linked Data

• MyVariant Identifiers: chr19:g.50333101T>G (hg19) ; chr19:g.49829844T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829844T>G , CM000681.2:g.49829844T>G	GRCh38
NC_000019.9:g.50333101T>G , CM000681.1:g.50333101T>G	GRCh37
NC_000019.8:g.55024913T>G	NCBI36
NG_017091.1:g.16566T>G , LRG_368:g.16566T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.584T>G	ENSP00000470692.3:p.Phe195Cys
ENST00000312865.10:c.584T>G MANE Select	ENSP00000326767.5:p.Phe195Cys
ENST00000538643.5:c.181-667T>G	ENSP00000437496.1:n.181-667T>G
ENST00000595185.5:c.584T>G	ENSP00000470027.1:p.Phe195Cys
ENST00000612791.4:c.584T>G	ENSP00000479851.1:p.Phe195Cys
ENST00000612854.4:c.450+829T>G	ENSP00000482155.1:n.450+829T>G
ENST00000617849.4:c.158-895T>G	ENSP00000484882.1:n.158-895T>G
ENST00000618715.4:c.158-894T>G	ENSP00000480731.1:n.158-894T>G
ENST00000620467.4:c.584T>G	ENSP00000482659.1:p.Phe195Cys
ENST00000622402.4:c.146-5983T>G	ENSP00000478074.1:n.146-5983T>G
NM_030973.3:c.584T>G , LRG_368t1:c.584T>G	NP_112235.2:p.Phe195Cys
XM_011527353.1:c.584T>G	XP_011525655.1:p.Phe195Cys
NM_001378355.1:c.584T>G	NP_001365284.1:p.Phe195Cys
NM_030973.4:c.584T>G MANE Select	NP_112235.2:p.Phe195Cys