Canonical Allele Identifier: CA2340605179

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830475_49830477delinsTCA , CM000681.2:g.49830475_49830477delinsTCA	GRCh38
NC_000019.9:g.50333732_50333734delinsTCA , CM000681.1:g.50333732_50333734delinsTCA	GRCh37
NC_000019.8:g.55025544_55025546delinsTCA	NCBI36
NG_017091.1:g.17197_17199delinsTCA , LRG_368:g.17197_17199delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-36_820-34delinsTCA	ENSP00000470692.3:n.820-36_820-34delinsTCA
ENST00000312865.10:c.820-36_820-34delinsTCA MANE Select	ENSP00000326767.5:n.820-36_820-34delinsTCA
ENST00000538643.5:c.181-36_181-34delinsTCA	ENSP00000437496.1:n.181-36_181-34delinsTCA
ENST00000595185.5:c.688+527_688+529delinsTCA	ENSP00000470027.1:n.688+527_688+529delinsTCA
ENST00000612791.4:c.761+313_761+315delinsTCA	ENSP00000479851.1:n.761+313_761+315delinsTCA
ENST00000612854.4:c.450+1460_450+1462delinsTCA	ENSP00000482155.1:n.450+1460_450+1462delinsTCA
ENST00000617849.4:c.158-264_158-262delinsTCA	ENSP00000484882.1:n.158-264_158-262delinsTCA
ENST00000618715.4:c.158-263_158-261delinsTCA	ENSP00000480731.1:n.158-263_158-261delinsTCA
ENST00000620467.4:c.820-36_820-34delinsTCA	ENSP00000482659.1:n.820-36_820-34delinsTCA
ENST00000622402.4:c.146-5352_146-5350delinsTCA	ENSP00000478074.1:n.146-5352_146-5350delinsTCA
NM_030973.3:c.820-36_820-34delinsTCA , LRG_368t1:c.820-36_820-34delinsTCA	NP_112235.2:n.820-36_820-34delinsTCA
XM_011527353.1:c.820-36_820-34delinsTCA	XP_011525655.1:n.820-36_820-34delinsTCA
NM_001378355.1:c.820-36_820-34delinsTCA	NP_001365284.1:n.820-36_820-34delinsTCA
NM_030973.4:c.820-36_820-34delinsTCA MANE Select	NP_112235.2:n.820-36_820-34delinsTCA