Canonical Allele Identifier: CA996720303

Gene: MED25

Linked Data

• dbSNP Id: rs2074046689
• gnomAD v3: 19-49830429-GGGT-G
• gnomAD v4: 19-49830429-GGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830434_49830436del , CM000681.2:g.49830434_49830436del	GRCh38
NC_000019.9:g.50333691_50333693del , CM000681.1:g.50333691_50333693del	GRCh37
NC_000019.8:g.55025503_55025505del	NCBI36
NG_017091.1:g.17156_17158del , LRG_368:g.17156_17158del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-77_820-75del	ENSP00000470692.3:n.820-77_820-75del
ENST00000312865.10:c.820-77_820-75del MANE Select	ENSP00000326767.5:n.820-77_820-75del
ENST00000538643.5:c.181-77_181-75del	ENSP00000437496.1:n.181-77_181-75del
ENST00000595185.5:c.688+486_688+488del	ENSP00000470027.1:n.688+486_688+488del
ENST00000612791.4:c.761+272_761+274del	ENSP00000479851.1:n.761+272_761+274del
ENST00000612854.4:c.450+1419_450+1421del	ENSP00000482155.1:n.450+1419_450+1421del
ENST00000617849.4:c.158-305_158-303del	ENSP00000484882.1:n.158-305_158-303del
ENST00000618715.4:c.158-304_158-302del	ENSP00000480731.1:n.158-304_158-302del
ENST00000620467.4:c.820-77_820-75del	ENSP00000482659.1:n.820-77_820-75del
ENST00000622402.4:c.146-5393_146-5391del	ENSP00000478074.1:n.146-5393_146-5391del
NM_030973.3:c.820-77_820-75del , LRG_368t1:c.820-77_820-75del	NP_112235.2:n.820-77_820-75del
XM_011527353.1:c.820-77_820-75del	XP_011525655.1:n.820-77_820-75del
NM_001378355.1:c.820-77_820-75del	NP_001365284.1:n.820-77_820-75del
NM_030973.4:c.820-77_820-75del MANE Select	NP_112235.2:n.820-77_820-75del