Canonical Allele Identifier: CA406913317

Gene: MED25

Linked Data

• dbSNP Id: rs1314169868
• gnomAD v2: 19-50333148-A-G
• gnomAD v4: 19-49829891-A-G
• MyVariant Identifiers: chr19:g.50333148A>G (hg19) ; chr19:g.49829891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829891A>G , CM000681.2:g.49829891A>G	GRCh38
NC_000019.9:g.50333148A>G , CM000681.1:g.50333148A>G	GRCh37
NC_000019.8:g.55024960A>G	NCBI36
NG_017091.1:g.16613A>G , LRG_368:g.16613A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.631A>G	ENSP00000470692.3:p.Thr211Ala
ENST00000312865.10:c.631A>G MANE Select	ENSP00000326767.5:p.Thr211Ala
ENST00000538643.5:c.181-620A>G	ENSP00000437496.1:n.181-620A>G
ENST00000595185.5:c.631A>G	ENSP00000470027.1:p.Thr211Ala
ENST00000612791.4:c.629A>G	ENSP00000479851.1:p.Asp210Gly
ENST00000612854.4:c.450+876A>G	ENSP00000482155.1:n.450+876A>G
ENST00000617849.4:c.158-848A>G	ENSP00000484882.1:n.158-848A>G
ENST00000618715.4:c.158-847A>G	ENSP00000480731.1:n.158-847A>G
ENST00000620467.4:c.631A>G	ENSP00000482659.1:p.Thr211Ala
ENST00000622402.4:c.146-5936A>G	ENSP00000478074.1:n.146-5936A>G
NM_030973.3:c.631A>G , LRG_368t1:c.631A>G	NP_112235.2:p.Thr211Ala
XM_011527353.1:c.631A>G	XP_011525655.1:p.Thr211Ala
NM_001378355.1:c.631A>G	NP_001365284.1:p.Thr211Ala
NM_030973.4:c.631A>G MANE Select	NP_112235.2:p.Thr211Ala