Canonical Allele Identifier: CA2340605290

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830688_49830690delinsCCA , CM000681.2:g.49830688_49830690delinsCCA	GRCh38
NC_000019.9:g.50333945_50333947delinsCCA , CM000681.1:g.50333945_50333947delinsCCA	GRCh37
NC_000019.8:g.55025757_55025759delinsCCA	NCBI36
NG_017091.1:g.17410_17412delinsCCA , LRG_368:g.17410_17412delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.908-6_908-4delinsCCA	ENSP00000470692.3:n.908-6_908-4delinsCCA
ENST00000312865.10:c.908-6_908-4delinsCCA MANE Select	ENSP00000326767.5:n.908-6_908-4delinsCCA
ENST00000538643.5:c.269-6_269-4delinsCCA	ENSP00000437496.1:n.269-6_269-4delinsCCA
ENST00000595185.5:c.688+740_688+742delinsCCA	ENSP00000470027.1:n.688+740_688+742delinsCCA
ENST00000612791.4:c.761+526_761+528delinsCCA	ENSP00000479851.1:n.761+526_761+528delinsCCA
ENST00000612854.4:c.450+1673_450+1675delinsCCA	ENSP00000482155.1:n.450+1673_450+1675delinsCCA
ENST00000617849.4:c.158-51_158-49delinsCCA	ENSP00000484882.1:n.158-51_158-49delinsCCA
ENST00000618715.4:c.158-50_158-48delinsCCA	ENSP00000480731.1:n.158-50_158-48delinsCCA
ENST00000620467.4:c.908-6_908-4delinsCCA	ENSP00000482659.1:n.908-6_908-4delinsCCA
ENST00000622402.4:c.146-5139_146-5137delinsCCA	ENSP00000478074.1:n.146-5139_146-5137delinsCCA
NM_030973.3:c.908-6_908-4delinsCCA , LRG_368t1:c.908-6_908-4delinsCCA	NP_112235.2:n.908-6_908-4delinsCCA
XM_011527353.1:c.908-6_908-4delinsCCA	XP_011525655.1:n.908-6_908-4delinsCCA
NM_001378355.1:c.908-6_908-4delinsCCA	NP_001365284.1:n.908-6_908-4delinsCCA
NM_030973.4:c.908-6_908-4delinsCCA MANE Select	NP_112235.2:n.908-6_908-4delinsCCA