Canonical Allele Identifier: CA2586449968
Gene: MED25 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49830450_49830463del , CM000681.2:g.49830450_49830463del GRCh38
NC_000019.9:g.50333707_50333720del , CM000681.1:g.50333707_50333720del GRCh37
NC_000019.8:g.55025519_55025532del NCBI36
NG_017091.1:g.17172_17185del , LRG_368:g.17172_17185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000593767.3:c.820-61_820-48del ENSP00000470692.3:n.820-61_820-48del
ENST00000312865.10:c.820-61_820-48del MANE Select ENSP00000326767.5:n.820-61_820-48del
ENST00000538643.5:c.181-61_181-48del ENSP00000437496.1:n.181-61_181-48del
ENST00000595185.5:c.688+502_688+515del ENSP00000470027.1:n.688+502_688+515del
ENST00000612791.4:c.761+288_761+301del ENSP00000479851.1:n.761+288_761+301del
ENST00000612854.4:c.450+1435_450+1448del ENSP00000482155.1:n.450+1435_450+1448del
ENST00000617849.4:c.158-289_158-276del ENSP00000484882.1:n.158-289_158-276del
ENST00000618715.4:c.158-288_158-275del ENSP00000480731.1:n.158-288_158-275del
ENST00000620467.4:c.820-61_820-48del ENSP00000482659.1:n.820-61_820-48del
ENST00000622402.4:c.146-5377_146-5364del ENSP00000478074.1:n.146-5377_146-5364del
NM_030973.3:c.820-61_820-48del , LRG_368t1:c.820-61_820-48del NP_112235.2:n.820-61_820-48del
XM_011527353.1:c.820-61_820-48del XP_011525655.1:n.820-61_820-48del
NM_001378355.1:c.820-61_820-48del NP_001365284.1:n.820-61_820-48del
NM_030973.4:c.820-61_820-48del MANE Select NP_112235.2:n.820-61_820-48del