Canonical Allele Identifier: CA2340605194

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830495_49830503delinsTCCCTTCTA , CM000681.2:g.49830495_49830503delinsTCCCTTCTA	GRCh38
NC_000019.9:g.50333752_50333760delinsTCCCTTCTA , CM000681.1:g.50333752_50333760delinsTCCCTTCTA	GRCh37
NC_000019.8:g.55025564_55025572delinsTCCCTTCTA	NCBI36
NG_017091.1:g.17217_17225delinsTCCCTTCTA , LRG_368:g.17217_17225delinsTCCCTTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-16_820-8delinsTCCCTTCTA	ENSP00000470692.3:n.820-16_820-8delinsTCCCTTCTA
ENST00000312865.10:c.820-16_820-8delinsTCCCTTCTA MANE Select	ENSP00000326767.5:n.820-16_820-8delinsTCCCTTCTA
ENST00000538643.5:c.181-16_181-8delinsTCCCTTCTA	ENSP00000437496.1:n.181-16_181-8delinsTCCCTTCTA
ENST00000595185.5:c.688+547_688+555delinsTCCCTTCTA	ENSP00000470027.1:n.688+547_688+555delinsTCCCTTCTA
ENST00000612791.4:c.761+333_761+341delinsTCCCTTCTA	ENSP00000479851.1:n.761+333_761+341delinsTCCCTTCTA
ENST00000612854.4:c.450+1480_450+1488delinsTCCCTTCTA	ENSP00000482155.1:n.450+1480_450+1488delinsTCCCTTCTA
ENST00000617849.4:c.158-244_158-236delinsTCCCTTCTA	ENSP00000484882.1:n.158-244_158-236delinsTCCCTTCTA
ENST00000618715.4:c.158-243_158-235delinsTCCCTTCTA	ENSP00000480731.1:n.158-243_158-235delinsTCCCTTCTA
ENST00000620467.4:c.820-16_820-8delinsTCCCTTCTA	ENSP00000482659.1:n.820-16_820-8delinsTCCCTTCTA
ENST00000622402.4:c.146-5332_146-5324delinsTCCCTTCTA	ENSP00000478074.1:n.146-5332_146-5324delinsTCCCTTCTA
NM_030973.3:c.820-16_820-8delinsTCCCTTCTA , LRG_368t1:c.820-16_820-8delinsTCCCTTCTA	NP_112235.2:n.820-16_820-8delinsTCCCTTCTA
XM_011527353.1:c.820-16_820-8delinsTCCCTTCTA	XP_011525655.1:n.820-16_820-8delinsTCCCTTCTA
NM_001378355.1:c.820-16_820-8delinsTCCCTTCTA	NP_001365284.1:n.820-16_820-8delinsTCCCTTCTA
NM_030973.4:c.820-16_820-8delinsTCCCTTCTA MANE Select	NP_112235.2:n.820-16_820-8delinsTCCCTTCTA