Canonical Allele Identifier: CA2340605181

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830478_49830480delinsCCA , CM000681.2:g.49830478_49830480delinsCCA	GRCh38
NC_000019.9:g.50333735_50333737delinsCCA , CM000681.1:g.50333735_50333737delinsCCA	GRCh37
NC_000019.8:g.55025547_55025549delinsCCA	NCBI36
NG_017091.1:g.17200_17202delinsCCA , LRG_368:g.17200_17202delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-33_820-31delinsCCA	ENSP00000470692.3:n.820-33_820-31delinsCCA
ENST00000312865.10:c.820-33_820-31delinsCCA MANE Select	ENSP00000326767.5:n.820-33_820-31delinsCCA
ENST00000538643.5:c.181-33_181-31delinsCCA	ENSP00000437496.1:n.181-33_181-31delinsCCA
ENST00000595185.5:c.688+530_688+532delinsCCA	ENSP00000470027.1:n.688+530_688+532delinsCCA
ENST00000612791.4:c.761+316_761+318delinsCCA	ENSP00000479851.1:n.761+316_761+318delinsCCA
ENST00000612854.4:c.450+1463_450+1465delinsCCA	ENSP00000482155.1:n.450+1463_450+1465delinsCCA
ENST00000617849.4:c.158-261_158-259delinsCCA	ENSP00000484882.1:n.158-261_158-259delinsCCA
ENST00000618715.4:c.158-260_158-258delinsCCA	ENSP00000480731.1:n.158-260_158-258delinsCCA
ENST00000620467.4:c.820-33_820-31delinsCCA	ENSP00000482659.1:n.820-33_820-31delinsCCA
ENST00000622402.4:c.146-5349_146-5347delinsCCA	ENSP00000478074.1:n.146-5349_146-5347delinsCCA
NM_030973.3:c.820-33_820-31delinsCCA , LRG_368t1:c.820-33_820-31delinsCCA	NP_112235.2:n.820-33_820-31delinsCCA
XM_011527353.1:c.820-33_820-31delinsCCA	XP_011525655.1:n.820-33_820-31delinsCCA
NM_001378355.1:c.820-33_820-31delinsCCA	NP_001365284.1:n.820-33_820-31delinsCCA
NM_030973.4:c.820-33_820-31delinsCCA MANE Select	NP_112235.2:n.820-33_820-31delinsCCA