Canonical Allele Identifier: CA406914660

Gene: MED25

Linked Data

• MyVariant Identifiers: chr19:g.50333840G>T (hg19) ; chr19:g.49830583G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830583G>T , CM000681.2:g.49830583G>T	GRCh38
NC_000019.9:g.50333840G>T , CM000681.1:g.50333840G>T	GRCh37
NC_000019.8:g.55025652G>T	NCBI36
NG_017091.1:g.17305G>T , LRG_368:g.17305G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.892G>T	ENSP00000470692.3:p.Gly298Trp
ENST00000312865.10:c.892G>T MANE Select	ENSP00000326767.5:p.Gly298Trp
ENST00000538643.5:c.253G>T	ENSP00000437496.1:p.Gly85Trp
ENST00000595185.5:c.688+635G>T	ENSP00000470027.1:n.688+635G>T
ENST00000612791.4:c.761+421G>T	ENSP00000479851.1:n.761+421G>T
ENST00000612854.4:c.450+1568G>T	ENSP00000482155.1:n.450+1568G>T
ENST00000617849.4:c.158-156G>T	ENSP00000484882.1:n.158-156G>T
ENST00000618715.4:c.158-155G>T	ENSP00000480731.1:n.158-155G>T
ENST00000620467.4:c.892G>T	ENSP00000482659.1:p.Gly298Trp
ENST00000622402.4:c.146-5244G>T	ENSP00000478074.1:n.146-5244G>T
NM_030973.3:c.892G>T , LRG_368t1:c.892G>T	NP_112235.2:p.Gly298Trp
XM_011527353.1:c.892G>T	XP_011525655.1:p.Gly298Trp
NM_001378355.1:c.892G>T	NP_001365284.1:p.Gly298Trp
NM_030973.4:c.892G>T MANE Select	NP_112235.2:p.Gly298Trp