Canonical Allele Identifier: CA2586449670

Gene: MED25

Linked Data

• gnomAD v4: 19-49829895-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829896dup , CM000681.2:g.49829896dup	GRCh38
NC_000019.9:g.50333153dup , CM000681.1:g.50333153dup	GRCh37
NC_000019.8:g.55024965dup	NCBI36
NG_017091.1:g.16618dup , LRG_368:g.16618dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.636dup	ENSP00000470692.3:p.Val213CysfsTer?
ENST00000312865.10:c.636dup MANE Select	ENSP00000326767.5:p.Val213CysfsTer?
ENST00000538643.5:c.181-615dup	ENSP00000437496.1:n.181-615dup
ENST00000595185.5:c.636dup	ENSP00000470027.1:p.Val213CysfsTer?
ENST00000612791.4:c.634dup	ENSP00000479851.1:p.Cys212LeufsTer2
ENST00000612854.4:c.450+881dup	ENSP00000482155.1:n.450+881dup
ENST00000617849.4:c.158-843dup	ENSP00000484882.1:n.158-843dup
ENST00000618715.4:c.158-842dup	ENSP00000480731.1:n.158-842dup
ENST00000620467.4:c.636dup	ENSP00000482659.1:p.Val213CysfsTer?
ENST00000622402.4:c.146-5931dup	ENSP00000478074.1:n.146-5931dup
NM_030973.3:c.636dup , LRG_368t1:c.636dup	NP_112235.2:p.Val213CysfsTer?
XM_011527353.1:c.636dup	XP_011525655.1:p.Val213CysfsTer?
NM_001378355.1:c.636dup	NP_001365284.1:p.Val213CysfsTer?
NM_030973.4:c.636dup MANE Select	NP_112235.2:p.Val213CysfsTer?