Canonical Allele Identifier: CA2586449982

Gene: MED25

Linked Data

• gnomAD v4: 19-49830470-GGTCCTCACCAGTCCCTTCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830471_49830490del , CM000681.2:g.49830471_49830490del	GRCh38
NC_000019.9:g.50333728_50333747del , CM000681.1:g.50333728_50333747del	GRCh37
NC_000019.8:g.55025540_55025559del	NCBI36
NG_017091.1:g.17193_17212del , LRG_368:g.17193_17212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-40_820-21del	ENSP00000470692.3:n.820-40_820-21del
ENST00000312865.10:c.820-40_820-21del MANE Select	ENSP00000326767.5:n.820-40_820-21del
ENST00000538643.5:c.181-40_181-21del	ENSP00000437496.1:n.181-40_181-21del
ENST00000595185.5:c.688+523_688+542del	ENSP00000470027.1:n.688+523_688+542del
ENST00000612791.4:c.761+309_761+328del	ENSP00000479851.1:n.761+309_761+328del
ENST00000612854.4:c.450+1456_450+1475del	ENSP00000482155.1:n.450+1456_450+1475del
ENST00000617849.4:c.158-268_158-249del	ENSP00000484882.1:n.158-268_158-249del
ENST00000618715.4:c.158-267_158-248del	ENSP00000480731.1:n.158-267_158-248del
ENST00000620467.4:c.820-40_820-21del	ENSP00000482659.1:n.820-40_820-21del
ENST00000622402.4:c.146-5356_146-5337del	ENSP00000478074.1:n.146-5356_146-5337del
NM_030973.3:c.820-40_820-21del , LRG_368t1:c.820-40_820-21del	NP_112235.2:n.820-40_820-21del
XM_011527353.1:c.820-40_820-21del	XP_011525655.1:n.820-40_820-21del
NM_001378355.1:c.820-40_820-21del	NP_001365284.1:n.820-40_820-21del
NM_030973.4:c.820-40_820-21del MANE Select	NP_112235.2:n.820-40_820-21del