Canonical Allele Identifier: CA2586450019

Gene: MED25

Linked Data

• gnomAD v4: 19-49830659-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49830659T>C , CM000681.2:g.49830659T>C	GRCh38
NC_000019.9:g.50333916T>C , CM000681.1:g.50333916T>C	GRCh37
NC_000019.8:g.55025728T>C	NCBI36
NG_017091.1:g.17381T>C , LRG_368:g.17381T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.908-35T>C	ENSP00000470692.3:n.908-35T>C
ENST00000312865.10:c.908-35T>C MANE Select	ENSP00000326767.5:n.908-35T>C
ENST00000538643.5:c.269-35T>C	ENSP00000437496.1:n.269-35T>C
ENST00000595185.5:c.688+711T>C	ENSP00000470027.1:n.688+711T>C
ENST00000612791.4:c.761+497T>C	ENSP00000479851.1:n.761+497T>C
ENST00000612854.4:c.450+1644T>C	ENSP00000482155.1:n.450+1644T>C
ENST00000617849.4:c.158-80T>C	ENSP00000484882.1:n.158-80T>C
ENST00000618715.4:c.158-79T>C	ENSP00000480731.1:n.158-79T>C
ENST00000620467.4:c.908-35T>C	ENSP00000482659.1:n.908-35T>C
ENST00000622402.4:c.146-5168T>C	ENSP00000478074.1:n.146-5168T>C
NM_030973.3:c.908-35T>C , LRG_368t1:c.908-35T>C	NP_112235.2:n.908-35T>C
XM_011527353.1:c.908-35T>C	XP_011525655.1:n.908-35T>C
NM_001378355.1:c.908-35T>C	NP_001365284.1:n.908-35T>C
NM_030973.4:c.908-35T>C MANE Select	NP_112235.2:n.908-35T>C