Canonical Allele Identifier: CA2586449964

Gene: MED25

Linked Data

• gnomAD v4: 19-49830443-CGTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830445_49830448del , CM000681.2:g.49830445_49830448del	GRCh38
NC_000019.9:g.50333702_50333705del , CM000681.1:g.50333702_50333705del	GRCh37
NC_000019.8:g.55025514_55025517del	NCBI36
NG_017091.1:g.17167_17170del , LRG_368:g.17167_17170del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.820-66_820-63del	ENSP00000470692.3:n.820-66_820-63del
ENST00000312865.10:c.820-66_820-63del MANE Select	ENSP00000326767.5:n.820-66_820-63del
ENST00000538643.5:c.181-66_181-63del	ENSP00000437496.1:n.181-66_181-63del
ENST00000595185.5:c.688+497_688+500del	ENSP00000470027.1:n.688+497_688+500del
ENST00000612791.4:c.761+283_761+286del	ENSP00000479851.1:n.761+283_761+286del
ENST00000612854.4:c.450+1430_450+1433del	ENSP00000482155.1:n.450+1430_450+1433del
ENST00000617849.4:c.158-294_158-291del	ENSP00000484882.1:n.158-294_158-291del
ENST00000618715.4:c.158-293_158-290del	ENSP00000480731.1:n.158-293_158-290del
ENST00000620467.4:c.820-66_820-63del	ENSP00000482659.1:n.820-66_820-63del
ENST00000622402.4:c.146-5382_146-5379del	ENSP00000478074.1:n.146-5382_146-5379del
NM_030973.3:c.820-66_820-63del , LRG_368t1:c.820-66_820-63del	NP_112235.2:n.820-66_820-63del
XM_011527353.1:c.820-66_820-63del	XP_011525655.1:n.820-66_820-63del
NM_001378355.1:c.820-66_820-63del	NP_001365284.1:n.820-66_820-63del
NM_030973.4:c.820-66_820-63del MANE Select	NP_112235.2:n.820-66_820-63del