Canonical Allele Identifier: CA14664066
Gene: MED25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49818843A>G , CM000681.2:g.49818843A>G GRCh38
NC_000019.9:g.50322100A>G , CM000681.1:g.50322100A>G GRCh37
NC_000019.8:g.55013912A>G NCBI36
NG_017091.1:g.5565A>G , LRG_368:g.5565A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000593767.3:c.180+227A>G ENSP00000470692.3:n.180+227A>G
ENST00000312865.10:c.180+227A>G MANE Select ENSP00000326767.5:n.180+227A>G
ENST00000538643.5:c.180+227A>G ENSP00000437496.1:n.180+227A>G
ENST00000593595.1:n.467A>G
ENST00000593636.1:n.233+227A>G
ENST00000595185.5:c.180+227A>G ENSP00000470027.1:n.180+227A>G
ENST00000612791.4:c.180+227A>G ENSP00000479851.1:n.180+227A>G
ENST00000612854.4:c.180+227A>G ENSP00000482155.1:n.180+227A>G
ENST00000617849.4:c.157+250A>G ENSP00000484882.1:n.157+250A>G
ENST00000618715.4:c.157+250A>G ENSP00000480731.1:n.157+250A>G
ENST00000620467.4:c.180+227A>G ENSP00000482659.1:n.180+227A>G
ENST00000622402.4:c.145+262A>G ENSP00000478074.1:n.145+262A>G
NM_030973.3:c.180+227A>G , LRG_368t1:c.180+227A>G NP_112235.2:n.180+227A>G
XM_011527353.1:c.180+227A>G XP_011525655.1:n.180+227A>G
NM_001378355.1:c.180+227A>G NP_001365284.1:n.180+227A>G
NM_030973.4:c.180+227A>G MANE Select NP_112235.2:n.180+227A>G