Canonical Allele Identifier: CA2576857188

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830469T>G , CM000681.2:g.49830469T>G	GRCh38
NC_000019.9:g.50333726T>G , CM000681.1:g.50333726T>G	GRCh37
NC_000019.8:g.55025538T>G	NCBI36
NG_017091.1:g.17191T>G , LRG_368:g.17191T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-42T>G	ENSP00000470692.3:n.820-42T>G
ENST00000312865.10:c.820-42T>G MANE Select	ENSP00000326767.5:n.820-42T>G
ENST00000538643.5:c.181-42T>G	ENSP00000437496.1:n.181-42T>G
ENST00000595185.5:c.688+521T>G	ENSP00000470027.1:n.688+521T>G
ENST00000612791.4:c.761+307T>G	ENSP00000479851.1:n.761+307T>G
ENST00000612854.4:c.450+1454T>G	ENSP00000482155.1:n.450+1454T>G
ENST00000617849.4:c.158-270T>G	ENSP00000484882.1:n.158-270T>G
ENST00000618715.4:c.158-269T>G	ENSP00000480731.1:n.158-269T>G
ENST00000620467.4:c.820-42T>G	ENSP00000482659.1:n.820-42T>G
ENST00000622402.4:c.146-5358T>G	ENSP00000478074.1:n.146-5358T>G
NM_030973.3:c.820-42T>G , LRG_368t1:c.820-42T>G	NP_112235.2:n.820-42T>G
XM_011527353.1:c.820-42T>G	XP_011525655.1:n.820-42T>G
NM_001378355.1:c.820-42T>G	NP_001365284.1:n.820-42T>G
NM_030973.4:c.820-42T>G MANE Select	NP_112235.2:n.820-42T>G