Canonical Allele Identifier: CA406911909

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49828450T>C , CM000681.2:g.49828450T>C	GRCh38
NC_000019.9:g.50331707T>C , CM000681.1:g.50331707T>C	GRCh37
NC_000019.8:g.55023519T>C	NCBI36
NG_017091.1:g.15172T>C , LRG_368:g.15172T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_030973.4:c.307T>C MANE Select	NP_112235.2:p.Phe103Leu
ENST00000312865.10:c.307T>C MANE Select	ENSP00000326767.5:p.Phe103Leu
NM_001378355.1:c.307T>C	NP_001365284.1:p.Phe103Leu
NM_030973.3:c.307T>C , LRG_368t1:c.307T>C	NP_112235.2:p.Phe103Leu
ENST00000538643.5:c.181-2061T>C	ENSP00000437496.1:n.181-2061T>C
ENST00000593767.3:c.307T>C	ENSP00000470692.3:p.Phe103Leu
ENST00000595185.5:c.307T>C	ENSP00000470027.1:p.Phe103Leu
ENST00000612791.4:c.307T>C	ENSP00000479851.1:p.Phe103Leu
ENST00000612854.4:c.307T>C	ENSP00000482155.1:p.Phe103Leu
ENST00000617849.4:c.158-2289T>C	ENSP00000484882.1:n.158-2289T>C
ENST00000618715.4:c.158-2288T>C	ENSP00000480731.1:n.158-2288T>C
ENST00000620467.4:c.307T>C	ENSP00000482659.1:p.Phe103Leu
ENST00000622402.4:c.146-7377T>C	ENSP00000478074.1:n.146-7377T>C
XM_011527353.1:c.307T>C	XP_011525655.1:p.Phe103Leu