Canonical Allele Identifier: CA9585092

Gene: MED25

Linked Data

• ClinVar Variation Id: 2157493
• ClinVar RCV Id: RCV003078128
• dbSNP Id: rs745821423
• ExAC: 19:50333958 C / A
• gnomAD v2: 19-50333958-C-A
• gnomAD v4: 19-49830701-C-A
• MyVariant Identifiers: chr19:g.50333958C>A (hg19) ; chr19:g.49830701C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830701C>A , CM000681.2:g.49830701C>A	GRCh38
NC_000019.9:g.50333958C>A , CM000681.1:g.50333958C>A	GRCh37
NC_000019.8:g.55025770C>A	NCBI36
NG_017091.1:g.17423C>A , LRG_368:g.17423C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.915C>A	ENSP00000470692.3:p.Pro305=
ENST00000312865.10:c.915C>A MANE Select	ENSP00000326767.5:p.Pro305=
ENST00000538643.5:c.276C>A	ENSP00000437496.1:p.Pro92=
ENST00000595185.5:c.688+753C>A	ENSP00000470027.1:n.688+753C>A
ENST00000612791.4:c.761+539C>A	ENSP00000479851.1:n.761+539C>A
ENST00000612854.4:c.450+1686C>A	ENSP00000482155.1:n.450+1686C>A
ENST00000617849.4:c.158-38C>A	ENSP00000484882.1:n.158-38C>A
ENST00000618715.4:c.158-37C>A	ENSP00000480731.1:n.158-37C>A
ENST00000620467.4:c.915C>A	ENSP00000482659.1:p.Pro305=
ENST00000622402.4:c.146-5126C>A	ENSP00000478074.1:n.146-5126C>A
NM_030973.3:c.915C>A , LRG_368t1:c.915C>A	NP_112235.2:p.Pro305=
XM_011527353.1:c.915C>A	XP_011525655.1:p.Pro305=
NM_001378355.1:c.915C>A	NP_001365284.1:p.Pro305=
NM_030973.4:c.915C>A MANE Select	NP_112235.2:p.Pro305=