Canonical Allele Identifier: CA633659105

Gene: MED25

Linked Data

• dbSNP Id: rs1283373868
• gnomAD v2: 19-50333735-CCA-C
• gnomAD v3: 19-49830478-CCA-C
• gnomAD v4: 19-49830478-CCA-C
• MyVariant Identifiers: chr19:g.50333736_50333737del (hg19) ; chr19:g.49830479_49830480del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830479_49830480del , CM000681.2:g.49830479_49830480del	GRCh38
NC_000019.9:g.50333736_50333737del , CM000681.1:g.50333736_50333737del	GRCh37
NC_000019.8:g.55025548_55025549del	NCBI36
NG_017091.1:g.17201_17202del , LRG_368:g.17201_17202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-32_820-31del	ENSP00000470692.3:n.820-32_820-31del
ENST00000312865.10:c.820-32_820-31del MANE Select	ENSP00000326767.5:n.820-32_820-31del
ENST00000538643.5:c.181-32_181-31del	ENSP00000437496.1:n.181-32_181-31del
ENST00000595185.5:c.688+531_688+532del	ENSP00000470027.1:n.688+531_688+532del
ENST00000612791.4:c.761+317_761+318del	ENSP00000479851.1:n.761+317_761+318del
ENST00000612854.4:c.450+1464_450+1465del	ENSP00000482155.1:n.450+1464_450+1465del
ENST00000617849.4:c.158-260_158-259del	ENSP00000484882.1:n.158-260_158-259del
ENST00000618715.4:c.158-259_158-258del	ENSP00000480731.1:n.158-259_158-258del
ENST00000620467.4:c.820-32_820-31del	ENSP00000482659.1:n.820-32_820-31del
ENST00000622402.4:c.146-5348_146-5347del	ENSP00000478074.1:n.146-5348_146-5347del
NM_030973.3:c.820-32_820-31del , LRG_368t1:c.820-32_820-31del	NP_112235.2:n.820-32_820-31del
XM_011527353.1:c.820-32_820-31del	XP_011525655.1:n.820-32_820-31del
NM_001378355.1:c.820-32_820-31del	NP_001365284.1:n.820-32_820-31del
NM_030973.4:c.820-32_820-31del MANE Select	NP_112235.2:n.820-32_820-31del