Canonical Allele Identifier: CA2340605192

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830492_49830497delinsTCTTCC , CM000681.2:g.49830492_49830497delinsTCTTCC	GRCh38
NC_000019.9:g.50333749_50333754delinsTCTTCC , CM000681.1:g.50333749_50333754delinsTCTTCC	GRCh37
NC_000019.8:g.55025561_55025566delinsTCTTCC	NCBI36
NG_017091.1:g.17214_17219delinsTCTTCC , LRG_368:g.17214_17219delinsTCTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-19_820-14delinsTCTTCC	ENSP00000470692.3:n.820-19_820-14delinsTCTTCC
ENST00000312865.10:c.820-19_820-14delinsTCTTCC MANE Select	ENSP00000326767.5:n.820-19_820-14delinsTCTTCC
ENST00000538643.5:c.181-19_181-14delinsTCTTCC	ENSP00000437496.1:n.181-19_181-14delinsTCTTCC
ENST00000595185.5:c.688+544_688+549delinsTCTTCC	ENSP00000470027.1:n.688+544_688+549delinsTCTTCC
ENST00000612791.4:c.761+330_761+335delinsTCTTCC	ENSP00000479851.1:n.761+330_761+335delinsTCTTCC
ENST00000612854.4:c.450+1477_450+1482delinsTCTTCC	ENSP00000482155.1:n.450+1477_450+1482delinsTCTTCC
ENST00000617849.4:c.158-247_158-242delinsTCTTCC	ENSP00000484882.1:n.158-247_158-242delinsTCTTCC
ENST00000618715.4:c.158-246_158-241delinsTCTTCC	ENSP00000480731.1:n.158-246_158-241delinsTCTTCC
ENST00000620467.4:c.820-19_820-14delinsTCTTCC	ENSP00000482659.1:n.820-19_820-14delinsTCTTCC
ENST00000622402.4:c.146-5335_146-5330delinsTCTTCC	ENSP00000478074.1:n.146-5335_146-5330delinsTCTTCC
NM_030973.3:c.820-19_820-14delinsTCTTCC , LRG_368t1:c.820-19_820-14delinsTCTTCC	NP_112235.2:n.820-19_820-14delinsTCTTCC
XM_011527353.1:c.820-19_820-14delinsTCTTCC	XP_011525655.1:n.820-19_820-14delinsTCTTCC
NM_001378355.1:c.820-19_820-14delinsTCTTCC	NP_001365284.1:n.820-19_820-14delinsTCTTCC
NM_030973.4:c.820-19_820-14delinsTCTTCC MANE Select	NP_112235.2:n.820-19_820-14delinsTCTTCC