Canonical Allele Identifier: CA406914817

Gene: MED25

Linked Data

• gnomAD v4: 19-49830706-C-G
• MyVariant Identifiers: chr19:g.50333963C>G (hg19) ; chr19:g.49830706C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830706C>G , CM000681.2:g.49830706C>G	GRCh38
NC_000019.9:g.50333963C>G , CM000681.1:g.50333963C>G	GRCh37
NC_000019.8:g.55025775C>G	NCBI36
NG_017091.1:g.17428C>G , LRG_368:g.17428C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.920C>G	ENSP00000470692.3:p.Thr307Ser
ENST00000312865.10:c.920C>G MANE Select	ENSP00000326767.5:p.Thr307Ser
ENST00000538643.5:c.281C>G	ENSP00000437496.1:p.Thr94Ser
ENST00000595185.5:c.688+758C>G	ENSP00000470027.1:n.688+758C>G
ENST00000612791.4:c.761+544C>G	ENSP00000479851.1:n.761+544C>G
ENST00000612854.4:c.450+1691C>G	ENSP00000482155.1:n.450+1691C>G
ENST00000617849.4:c.158-33C>G	ENSP00000484882.1:n.158-33C>G
ENST00000618715.4:c.158-32C>G	ENSP00000480731.1:n.158-32C>G
ENST00000620467.4:c.920C>G	ENSP00000482659.1:p.Thr307Ser
ENST00000622402.4:c.146-5121C>G	ENSP00000478074.1:n.146-5121C>G
NM_030973.3:c.920C>G , LRG_368t1:c.920C>G	NP_112235.2:p.Thr307Ser
XM_011527353.1:c.920C>G	XP_011525655.1:p.Thr307Ser
NM_001378355.1:c.920C>G	NP_001365284.1:p.Thr307Ser
NM_030973.4:c.920C>G MANE Select	NP_112235.2:p.Thr307Ser